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The Viability of Short Stems in Total Hip Arthroplasty

The Viability of Short Stems in Total Hip Arthroplasty

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02577822
Enrollment
60
Registered
2015-10-16
Start date
2013-10-31
Completion date
2019-07-31
Last updated
2020-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis of Hip

Brief summary

The purpose of this study is to determine the viability of short femoral stems as an alternative to standard-length stems in total hip arthroplasty.

Detailed description

Porous-coated cementless stems were introduced in the late 1970s, in response to the high incidence of aseptic loosening associated with cemented stems (Judet et al 1978, Kavanagh et al 1989, Lord 1982, Stauffer 1982). The stem's porous surface achieves fixation via bony ingrowth at the endosteum (Engh et al 1987). In an effort to mimic the femur's natural stress distribution, many designs preferentially load the metaphysis (Joshi et al 2000). One such design is the proximally coated titanium tapered wedge, which is widely used today (Pitto et al 2010). Because loading is primarily dictated by bony ingrowth, the proximal porous coating avoids fixation at the diaphysis. The flat, tapered geometry reduces stiffness compared to cylindrical stems, thereby propagating stress to the proximal femur, rather than down the stem's axis (Engh et al 1987, Harvey et al 1999), (Boehm 1998). Further contributing to decreased stiffness is titanium's low elastic modulus, relative to that of cobalt-chromium (Harvey et al 1999, Mulliken et al 1996). Some contend the need for distal fixation in Dorr type C hips due to thin cortical bone at the metaphysis; however, proximally engaging stems have been shown to perform well in these patients (Kelly et al 2007, Reitman et al 2003). If a stem's objective is to load proximally, then perhaps it need not extend into the diaphyseal canal. The emergence of short stems has initiated an alternative means of proximal loading, without the disruption of diaphyseal bone stock. The smaller incisions involved with short stem total hip arthroplasty (THA) reduce damage to muscle and soft tissue (Molli et al 2012). This enables a faster, more complete recovery for the patient, as well as a cosmetically superior result (Sherry et al 2003). Additionally, the preservation of bioavailable bone can be advantageous if a revision surgery is required (Toth et al 2010). Because short stems do not extend into the diaphysis, issues regarding proximal-distal mismatch of the femur are avoided (Patel et al 2013). This eases implantation and reduces the risk of intraoperative fracture (Azzam et al 2010, Cooper & Rodriguez 2010). The risk of intraoperative fracture is further mitigated because short stem THA does not require the use of reamers (Molli et al 2012, Scott et al 1975, Taylor et al 1978). Although the standard-length proximally coated titanium tapered wedge has a successful long-term track record, its design leaves room for improvement (Mallory et al 2001, Marshall et al 2004). Standard length stems cause stress-shielding in Gruen zones 1 and 7, suggesting that the diaphyseal portion of a stem may interfere with proximal loading (Gibbons et al 2001, Schmidt et al 2004). Even proximally coated flat tapered stems are subject to diaphyseal loading (Cooper et al 2011). The Accolade stem has been associated with significant early subsidence, especially in males with Dorr type A hips (Jacobs & Christensen 2009). This suggests that the stem may wedge distally, thereby interfering with osseointegration (White et al 2012). By achieving a purely metaphyseal fit, short stems can prevent excessive bone loss secondary to stress shielding (Gustke 2012). The investigators believe short stems are an equally effective alternative to traditional tapered stems in THA; however, long-term studies are essential to proving their efficacy. Long-term studies of short stems are lacking in current literature. With respect to initial stability and bony ingrowth, short-term data is promising; however, there is still potential for late aseptic failure (Capello et al 2009, Kroell et al 2009, Morales de Cano et al 2013, Schmidutz et al 2012). By conducting a single blinded, prospective, randomized investigation of two stems of varying length with equal metallurgy, coating, and proximal geometry, the investigators can identify the effects of stem length on long-term outcomes.

Interventions

DEVICETaperloc standard length stem
DEVICETaperloc short length stem

Sponsors

Northwestern University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Must require a total hip arthroplasty. * Ages 18-85 years, regardless of gender, ethnicity, or pathology

Exclusion criteria

* This study excludes any populations at risk. * Minors, as well as any persons unable to consent, will not be eligible.

Design outcomes

Primary

MeasureTime frameDescription
Mean VR-12 Mental Composite Score Through 2 Years Post OperativeAssesed pre-operatively, 6 weeks post-operatively, 3 months post-operatively, 6 months post-operatively, 12 months post-operatively, and 2 years post-operatively.Veteran's RAND 12 Item Health Survey used to assess health-related quality of life, to estimate disease burden, and to evaluate disease-specific benchmarks. Scores for the Mental Composite Score (MCS) range from 5.2 to 76.3 and are evaluated as a summative T-score with population mean of 50 (Standard Deviation = 10);higher scores indicate improved mental wellness/function as reported by patients.
Mean VR-12 Physical Composite Score Through 2 Years Post OperativeAssessed pre-operatively, 6 weeks post-operatively, 3 months post-operatively, 6 months post-operatively, 12 months post-operatively, and 2 years post-operatively.Veteran's RAND 12 Item Health Survey used to assess health-related quality of life, to estimate disease burden, and to evaluate disease-specific benchmarks. Scores for the Physical Composite Score (PCS) range from 6.3 to 71.8 and are evaluated as a summative T-score with population mean of 50 (Standard Deviation = 10);higher scores indicate improved mental wellness/function as reported by patients.
PROMIS Computerized Adaptive Tests (CATs) for Pain Behavior Through 2 Years Post-operativePre-operatively, 6 weeks post-operatively, 3 months post-operatively, 6 months post-operatively, 12 months post-operatively, and 2 years post-operatively.Patient-reported outcome (PRO) measures use answers that patients provide to questions to produce numeric values which indicate patients' state of wellbeing or suffering as well as their ability or lack of ability to function. Values are reported as T-scores with a reference population mean of 50 (SD=10); for the Pain Behavior domain higher scores indicate more frequent and severe incidence of pain during daily activities
PROMIS Computerized Adaptive Tests (CATs) for Physical Function Through 2 Years Post-operativePre-operatively, 6 weeks post-operatively, 3 months post-operatively, 6 months post-operatively, 12 months post-operatively, and 2 years post-operatively.Patient-reported outcome (PRO) measures use answers that patients provide to questions to produce numeric values which indicate patients' state of wellbeing or suffering as well as their ability or lack of ability to function. Values are reported as T-scores with a reference population mean of 50 (SD=10); for the Physical Function domain higher scores indicated improved physical function as reported by the patient
PROMIS Computerized Adaptive Tests (CATs) for Pain Interference Through 2 Years Post-operativePre-operatively, 6 weeks post-operatively, 3 months post-operatively, 6 months post-operatively, 12 months post-operatively, and 2 years post-operatively.Patient-reported outcome (PRO) measures use answers that patients provide to questions to produce numeric values which indicate patients' state of wellbeing or suffering as well as their ability or lack of ability to function. Values are reported as T-scores with a reference population mean of 50 (SD=10); for the Pain Interference domain higher scores indicated greater impact on patient's ability to perform daily activities and social function

Secondary

MeasureTime frameDescription
EBRA (Ein-Bild-Roentgen-Analyse) Femoral Component Analysis (EBRA-FCA) of Implant Subsidence Through 2 Years Post OperativeAssessed 6 weeks post-operatively, 6 months post-operatively, 12 months post-operatively, and 2 years post-operatively.EBRA-FCA is a commonly employed technique to evaluate implant migration via radiographic measurements taken over the duration of recovery. The mean subsidence values measured in millimeters were recorded for both the short and standard stem cohorts at each of the clinic visits for SOC. Of note, the individual responsible for performing and recording these measurements could not be reached during upload of the final study data and consequently the dispersion values for this measure were not available at the time of publication. The dispersion values for these measures have been recorded as '0' for each time point pending any response from the individual to obtain the original data.

Countries

United States

Participant flow

Participants by arm

ArmCount
Short Stem Group
Short femoral stem Taperloc short length stem
27
Long Stem Group
standard-length stem Taperloc standard length stem
33
Total60

Baseline characteristics

CharacteristicShort Stem GroupTotalLong Stem Group
Age, Continuous61.28 years
STANDARD_DEVIATION 10.73
60.47 years
STANDARD_DEVIATION 11.76
58.70 years
STANDARD_DEVIATION 11.99
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants2 Participants2 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
25 Participants55 Participants30 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
2 Participants3 Participants1 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants1 Participants1 Participants
Race (NIH/OMB)
Black or African American
12 Participants21 Participants9 Participants
Race (NIH/OMB)
More than one race
1 Participants6 Participants5 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants2 Participants2 Participants
Race (NIH/OMB)
White
14 Participants30 Participants16 Participants
Region of Enrollment
United States
27 participants60 participants33 participants
Sex: Female, Male
Female
15 Participants32 Participants17 Participants
Sex: Female, Male
Male
12 Participants28 Participants16 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 00 / 0
other
Total, other adverse events
0 / 00 / 0
serious
Total, serious adverse events
0 / 00 / 0

Outcome results

Primary

Mean VR-12 Mental Composite Score Through 2 Years Post Operative

Veteran's RAND 12 Item Health Survey used to assess health-related quality of life, to estimate disease burden, and to evaluate disease-specific benchmarks. Scores for the Mental Composite Score (MCS) range from 5.2 to 76.3 and are evaluated as a summative T-score with population mean of 50 (Standard Deviation = 10);higher scores indicate improved mental wellness/function as reported by patients.

Time frame: Assesed pre-operatively, 6 weeks post-operatively, 3 months post-operatively, 6 months post-operatively, 12 months post-operatively, and 2 years post-operatively.

Population: Discrepancies between the total number of patients analyzed and patients included in participant flow is due to patients lost to follow-up during the course of the study despite attempts to contact them by the research team

ArmMeasureGroupValue (MEAN)Dispersion
Short Stem GroupMean VR-12 Mental Composite Score Through 2 Years Post OperativeVR-12 MCS Mean Score (Pre-Op)47.3 T-ScoreStandard Deviation 11.3
Short Stem GroupMean VR-12 Mental Composite Score Through 2 Years Post OperativeVR-12 MCS Mean Score (6 wk)54.9 T-ScoreStandard Deviation 8.9
Short Stem GroupMean VR-12 Mental Composite Score Through 2 Years Post OperativeVR-12 MCS Mean Score (3 mo)56.4 T-ScoreStandard Deviation 11.2
Short Stem GroupMean VR-12 Mental Composite Score Through 2 Years Post OperativeVR-12 MCS Mean Score (6 mo)54.8 T-ScoreStandard Deviation 10.2
Short Stem GroupMean VR-12 Mental Composite Score Through 2 Years Post OperativeVR-12 MCS Mean Score (1 yr)53.0 T-ScoreStandard Deviation 9.6
Short Stem GroupMean VR-12 Mental Composite Score Through 2 Years Post OperativeVR-12 MCS Mean Score (2 yr)52.3 T-ScoreStandard Deviation 9.9
Long Stem GroupMean VR-12 Mental Composite Score Through 2 Years Post OperativeVR-12 MCS Mean Score (1 yr)56.7 T-ScoreStandard Deviation 8.3
Long Stem GroupMean VR-12 Mental Composite Score Through 2 Years Post OperativeVR-12 MCS Mean Score (Pre-Op)50.6 T-ScoreStandard Deviation 13.8
Long Stem GroupMean VR-12 Mental Composite Score Through 2 Years Post OperativeVR-12 MCS Mean Score (6 mo)56.4 T-ScoreStandard Deviation 9.3
Long Stem GroupMean VR-12 Mental Composite Score Through 2 Years Post OperativeVR-12 MCS Mean Score (6 wk)53.8 T-ScoreStandard Deviation 11.7
Long Stem GroupMean VR-12 Mental Composite Score Through 2 Years Post OperativeVR-12 MCS Mean Score (2 yr)55.3 T-ScoreStandard Deviation 9.9
Long Stem GroupMean VR-12 Mental Composite Score Through 2 Years Post OperativeVR-12 MCS Mean Score (3 mo)56.9 T-ScoreStandard Deviation 10.6
Primary

Mean VR-12 Physical Composite Score Through 2 Years Post Operative

Veteran's RAND 12 Item Health Survey used to assess health-related quality of life, to estimate disease burden, and to evaluate disease-specific benchmarks. Scores for the Physical Composite Score (PCS) range from 6.3 to 71.8 and are evaluated as a summative T-score with population mean of 50 (Standard Deviation = 10);higher scores indicate improved mental wellness/function as reported by patients.

Time frame: Assessed pre-operatively, 6 weeks post-operatively, 3 months post-operatively, 6 months post-operatively, 12 months post-operatively, and 2 years post-operatively.

Population: Discrepancies between the total number of patients analyzed and patients included in participant flow is due to patients lost to follow-up during the course of the study despite attempts to contact them by the research team

ArmMeasureGroupValue (MEAN)Dispersion
Short Stem GroupMean VR-12 Physical Composite Score Through 2 Years Post OperativeVR-12 PCS Mean Score (Pre-Op)25.2 T-ScoreStandard Deviation 6.8
Short Stem GroupMean VR-12 Physical Composite Score Through 2 Years Post OperativeVR-12 PCS Mean Score (6 wk)37.0 T-ScoreStandard Deviation 10
Short Stem GroupMean VR-12 Physical Composite Score Through 2 Years Post OperativeVR-12 PCS Mean Score (3 mo)42.1 T-ScoreStandard Deviation 10.2
Short Stem GroupMean VR-12 Physical Composite Score Through 2 Years Post OperativeVR-12 PCS Mean Score (6 mo)45.8 T-ScoreStandard Deviation 10
Short Stem GroupMean VR-12 Physical Composite Score Through 2 Years Post OperativeVR-12 PCS Mean Score (1 yr)48.7 T-ScoreStandard Deviation 10.9
Short Stem GroupMean VR-12 Physical Composite Score Through 2 Years Post OperativeVR-12 PCS Mean Score (2 yr)45.1 T-ScoreStandard Deviation 11.3
Long Stem GroupMean VR-12 Physical Composite Score Through 2 Years Post OperativeVR-12 PCS Mean Score (1 yr)49.5 T-ScoreStandard Deviation 8.3
Long Stem GroupMean VR-12 Physical Composite Score Through 2 Years Post OperativeVR-12 PCS Mean Score (Pre-Op)23.6 T-ScoreStandard Deviation 5.3
Long Stem GroupMean VR-12 Physical Composite Score Through 2 Years Post OperativeVR-12 PCS Mean Score (6 mo)44.7 T-ScoreStandard Deviation 9.5
Long Stem GroupMean VR-12 Physical Composite Score Through 2 Years Post OperativeVR-12 PCS Mean Score (6 wk)37.8 T-ScoreStandard Deviation 9.8
Long Stem GroupMean VR-12 Physical Composite Score Through 2 Years Post OperativeVR-12 PCS Mean Score (2 yr)48.5 T-ScoreStandard Deviation 5.2
Long Stem GroupMean VR-12 Physical Composite Score Through 2 Years Post OperativeVR-12 PCS Mean Score (3 mo)40.1 T-ScoreStandard Deviation 10.6
Primary

PROMIS Computerized Adaptive Tests (CATs) for Pain Behavior Through 2 Years Post-operative

Patient-reported outcome (PRO) measures use answers that patients provide to questions to produce numeric values which indicate patients' state of wellbeing or suffering as well as their ability or lack of ability to function. Values are reported as T-scores with a reference population mean of 50 (SD=10); for the Pain Behavior domain higher scores indicate more frequent and severe incidence of pain during daily activities

Time frame: Pre-operatively, 6 weeks post-operatively, 3 months post-operatively, 6 months post-operatively, 12 months post-operatively, and 2 years post-operatively.

Population: Discrepancies between the total number of patients analyzed and patients included in participant flow is due to patients lost to follow-up during the course of the study despite attempts to contact them by the research team

ArmMeasureGroupValue (MEAN)Dispersion
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Behavior Through 2 Years Post-operativePain Behavior T-Score (Pre-Op)59.2 T-ScoreStandard Deviation 6.5
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Behavior Through 2 Years Post-operativePain Behavior T-Score (6 wk)51.9 T-ScoreStandard Deviation 9.1
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Behavior Through 2 Years Post-operativePain Behavior T-Score (3 mo)48.0 T-ScoreStandard Deviation 10.1
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Behavior Through 2 Years Post-operativePain Behavior T-Score (6 mo)47.6 T-ScoreStandard Deviation 10.5
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Behavior Through 2 Years Post-operativePain Behavior T-Score (1 yr)45.2 T-ScoreStandard Deviation 11
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Behavior Through 2 Years Post-operativePain Behavior T-Score (2 yr)43.8 T-ScoreStandard Deviation 10.8
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Behavior Through 2 Years Post-operativePain Behavior T-Score (1 yr)45.2 T-ScoreStandard Deviation 9.8
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Behavior Through 2 Years Post-operativePain Behavior T-Score (Pre-Op)61.3 T-ScoreStandard Deviation 4.2
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Behavior Through 2 Years Post-operativePain Behavior T-Score (6 mo)47.4 T-ScoreStandard Deviation 10.8
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Behavior Through 2 Years Post-operativePain Behavior T-Score (6 wk)51.0 T-ScoreStandard Deviation 10.4
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Behavior Through 2 Years Post-operativePain Behavior T-Score (2 yr)40.3 T-ScoreStandard Deviation 8.7
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Behavior Through 2 Years Post-operativePain Behavior T-Score (3 mo)52.0 T-ScoreStandard Deviation 8.8
Primary

PROMIS Computerized Adaptive Tests (CATs) for Pain Interference Through 2 Years Post-operative

Patient-reported outcome (PRO) measures use answers that patients provide to questions to produce numeric values which indicate patients' state of wellbeing or suffering as well as their ability or lack of ability to function. Values are reported as T-scores with a reference population mean of 50 (SD=10); for the Pain Interference domain higher scores indicated greater impact on patient's ability to perform daily activities and social function

Time frame: Pre-operatively, 6 weeks post-operatively, 3 months post-operatively, 6 months post-operatively, 12 months post-operatively, and 2 years post-operatively.

Population: Discrepancies between the total number of patients analyzed and patients included in participant flow is due to patients lost to follow-up during the course of the study despite attempts to contact them by the research team

ArmMeasureGroupValue (MEAN)Dispersion
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Interference Through 2 Years Post-operativePain Interference T-Score (Pre-Op)64.6 T-ScoreStandard Deviation 8.6
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Interference Through 2 Years Post-operativePain Interference T-Score (6 wk)51.7 T-ScoreStandard Deviation 10.3
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Interference Through 2 Years Post-operativePain Interference T-Score (3 mo)49.7 T-ScoreStandard Deviation 10.1
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Interference Through 2 Years Post-operativePain Interference T-Score (6 mo)47.9 T-ScoreStandard Deviation 9.8
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Interference Through 2 Years Post-operativePain Interference T-Score (1 yr)48.00 T-ScoreStandard Deviation 10.5
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Interference Through 2 Years Post-operativePain Interference T-Score (2 yr)46.7 T-ScoreStandard Deviation 10.5
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Interference Through 2 Years Post-operativePain Interference T-Score (1 yr)44.0 T-ScoreStandard Deviation 8.3
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Interference Through 2 Years Post-operativePain Interference T-Score (Pre-Op)67.4 T-ScoreStandard Deviation 6.5
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Interference Through 2 Years Post-operativePain Interference T-Score (6 mo)46.6 T-ScoreStandard Deviation 10.6
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Interference Through 2 Years Post-operativePain Interference T-Score (6 wk)53.1 T-ScoreStandard Deviation 9.6
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Interference Through 2 Years Post-operativePain Interference T-Score (2 yr)42.2 T-ScoreStandard Deviation 6
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Pain Interference Through 2 Years Post-operativePain Interference T-Score (3 mo)51.1 T-ScoreStandard Deviation 10.1
Primary

PROMIS Computerized Adaptive Tests (CATs) for Physical Function Through 2 Years Post-operative

Patient-reported outcome (PRO) measures use answers that patients provide to questions to produce numeric values which indicate patients' state of wellbeing or suffering as well as their ability or lack of ability to function. Values are reported as T-scores with a reference population mean of 50 (SD=10); for the Physical Function domain higher scores indicated improved physical function as reported by the patient

Time frame: Pre-operatively, 6 weeks post-operatively, 3 months post-operatively, 6 months post-operatively, 12 months post-operatively, and 2 years post-operatively.

Population: Discrepancies between the total number of patients analyzed and patients included in participant flow is due to patients lost to follow-up during the course of the study despite attempts to contact them by the research team

ArmMeasureGroupValue (MEAN)Dispersion
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Physical Function Through 2 Years Post-operativePhysical Function T-Score (6 wk)41.00 T-ScoreStandard Deviation 7.8
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Physical Function Through 2 Years Post-operativePhysical Function T-Score (6 mo)47.4 T-ScoreStandard Deviation 8.6
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Physical Function Through 2 Years Post-operativePhysical Function T-Score (Pre-Op)29.6 T-ScoreStandard Deviation 5.8
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Physical Function Through 2 Years Post-operativePhysical Function T-Score (1 yr)48.3 T-ScoreStandard Deviation 8.8
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Physical Function Through 2 Years Post-operativePhysical Function T-Score (2 yr)52.9 T-ScoreStandard Deviation 12.1
Short Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Physical Function Through 2 Years Post-operativePhysical Function T-Score (3 mo)45.5 T-ScoreStandard Deviation 8.3
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Physical Function Through 2 Years Post-operativePhysical Function T-Score (2 yr)53.9 T-ScoreStandard Deviation 9.7
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Physical Function Through 2 Years Post-operativePhysical Function T-Score (Pre-Op)31.7 T-ScoreStandard Deviation 6.2
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Physical Function Through 2 Years Post-operativePhysical Function T-Score (6 wk)42.6 T-ScoreStandard Deviation 8
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Physical Function Through 2 Years Post-operativePhysical Function T-Score (3 mo)45.4 T-ScoreStandard Deviation 9.5
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Physical Function Through 2 Years Post-operativePhysical Function T-Score (6 mo)47.9 T-ScoreStandard Deviation 8
Long Stem GroupPROMIS Computerized Adaptive Tests (CATs) for Physical Function Through 2 Years Post-operativePhysical Function T-Score (1 yr)51.1 T-ScoreStandard Deviation 7.1
Secondary

EBRA (Ein-Bild-Roentgen-Analyse) Femoral Component Analysis (EBRA-FCA) of Implant Subsidence Through 2 Years Post Operative

EBRA-FCA is a commonly employed technique to evaluate implant migration via radiographic measurements taken over the duration of recovery. The mean subsidence values measured in millimeters were recorded for both the short and standard stem cohorts at each of the clinic visits for SOC. Of note, the individual responsible for performing and recording these measurements could not be reached during upload of the final study data and consequently the dispersion values for this measure were not available at the time of publication. The dispersion values for these measures have been recorded as '0' for each time point pending any response from the individual to obtain the original data.

Time frame: Assessed 6 weeks post-operatively, 6 months post-operatively, 12 months post-operatively, and 2 years post-operatively.

ArmMeasureGroupValue (MEAN)Dispersion
Short Stem GroupEBRA (Ein-Bild-Roentgen-Analyse) Femoral Component Analysis (EBRA-FCA) of Implant Subsidence Through 2 Years Post OperativeFemoral Stem Subsidence (6 wk)0.124 millimetersStandard Deviation 0.961
Short Stem GroupEBRA (Ein-Bild-Roentgen-Analyse) Femoral Component Analysis (EBRA-FCA) of Implant Subsidence Through 2 Years Post OperativeFemoral Stem Subsidence (6 mo)0.448 millimetersStandard Deviation 1.2
Short Stem GroupEBRA (Ein-Bild-Roentgen-Analyse) Femoral Component Analysis (EBRA-FCA) of Implant Subsidence Through 2 Years Post OperativeFemoral Stem Subsidence (1 yr)0.526 millimetersStandard Deviation 1.653
Short Stem GroupEBRA (Ein-Bild-Roentgen-Analyse) Femoral Component Analysis (EBRA-FCA) of Implant Subsidence Through 2 Years Post OperativeFemoral Stem Subsidence (2 yr)0.590 millimetersStandard Deviation 1.072
Long Stem GroupEBRA (Ein-Bild-Roentgen-Analyse) Femoral Component Analysis (EBRA-FCA) of Implant Subsidence Through 2 Years Post OperativeFemoral Stem Subsidence (2 yr)1.414 millimetersStandard Deviation 1.547
Long Stem GroupEBRA (Ein-Bild-Roentgen-Analyse) Femoral Component Analysis (EBRA-FCA) of Implant Subsidence Through 2 Years Post OperativeFemoral Stem Subsidence (6 wk)0.193 millimetersStandard Deviation 0.533
Long Stem GroupEBRA (Ein-Bild-Roentgen-Analyse) Femoral Component Analysis (EBRA-FCA) of Implant Subsidence Through 2 Years Post OperativeFemoral Stem Subsidence (1 yr)1.303 millimetersStandard Deviation 1.264
Long Stem GroupEBRA (Ein-Bild-Roentgen-Analyse) Femoral Component Analysis (EBRA-FCA) of Implant Subsidence Through 2 Years Post OperativeFemoral Stem Subsidence (6 mo)0.702 millimetersStandard Deviation 1.08

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026