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Comparison of Two Cementing Techniques of the Femoral Component in a Hip Prosthesis

Comparison of Two Cementing Techniques of the Femoral Component in a Hip Prosthesis. A Randomized Single-blind Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01952067
Enrollment
48
Registered
2013-09-27
Start date
2013-03-31
Completion date
2017-06-20
Last updated
2022-05-04

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

Conditions

Osteoarthritis, Hip

Keywords

Hip Prosthesis, surgery, cements, Radiostereometric Analysis

Brief summary

The primary aim of the study is to compare migration of the cemented Corail stem representing polished surfaced versions of the femoral stem. Two different methods will be used for reaming the femoral canal and cementing of the stem. Radiostereometric analysis (RSA) will be used in migration measurements. Furthermore pain, postoperative outcome and patient satisfaction will be assessed.

Interventions

PROCEDUREline-to-line reaming and cementing technique
PROCEDUREstandard over-reaming with 2 broach sizes

Sponsors

Kristiansund Hospital
CollaboratorOTHER
St. Olavs Hospital
CollaboratorOTHER
Norwegian University of Science and Technology
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
55 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients requiring cemented primary total hip replacement. * Patients with a diagnosis of osteoarthritis, avascular necrosis or post-traumatic arthritis * Patients who understand the conditions of the study and are willing and able to comply with the post-operative scheduled clinical and radiographic evaluations and the prescribed rehabilitation * Patient who signed the Ethics Committee approved specific Informed Consent Form prior to surgery

Exclusion criteria

* Patients who require revision of a previously implanted total hip replacement (THR) * Patients who will receive a THR without cement * Patients who have had a prior procedure of osteotomy on the femur * Obese patients where obesity is severe enough to affect subject's ability to perform activities of daily living (body mass index, kg/m2: BMI \>35) * Patients with active or suspected infection * Patients with malignancy

Design outcomes

Primary

MeasureTime frameDescription
Difference in subsidence of femoral stems of 200 micronschange from 6th day postoperative to 24 monthsRadiostereometric analysis (RSA) of implant migration: difference in translation and rotation (x-, y-, and z- axis) of the femoral stem

Secondary

MeasureTime frameDescription
Oxford Hip Scorechange from 6th day postoperative to 24 months12 questions. Every question is scored 4 to 0 according to the selected response. Thus it is a continuous score ranging from 48-0. Each of the 12 questions on the Oxford hip score is scored in the same way with the score decreasing as the reported symptoms increase (ie. become worse). All questions are laid out similarly with response categories denoting least (or no) symptoms being to the left of the page (scoring 4) and those representing greatest severity lying on the right hand side (scoring 0).
EQ-5D-5Lchange from 6th day postoperative to 24 months5 questions. Every question is scored 1 to 5 where 5 is worse outcome. For example one profile could be' 12233' We then convert this specific health state to an index value specific for that country. The index value calculator can be downloaded from the EuroQol Office. 5 questions. Every question is scored 1 to 5 where 5 is worse outcome. For example one profile could be' 12233' We then convert this specific health state to an index value specific for that country. The index value calculator can be downloaded from the EuroQol Office.
Harris Hip Score (HHS)change from 6th day postoperative to 24 monthsFour subscales make up HHS. The first is pain, which measures pain severity (44 points); function, which is made up of daily activities and gait (47 points); the absence of deformity, which is a subscale that measures hip flexion, adduction, internal rotation, leg length discrepancy and range of motion measures.(4 points), and range of motion (5 points). The survey has 10 question items and scores range from 0-100 with higher scores representing less dysfunction and better outcomes.
Visual Assessment Scale (VAS) for painchange from 6th day postoperative to 24 monthsA horizontal or vertical 10 cm line labelled at each end by descriptors such as 'no pain' and 'worse pain ever'. The patient marks the line to indicate pain severity and it is simply quantified by measuring the distance in cm from 0 (no pain) to the patient's marked rating.
Merle D'Aubigne scalechange from 6th day postoperative to 24 monthsThe score includes the parameters pain, mobility, and ability to walk, with each rated from 0 points (worst condition) to 6 points (best condition). Addition of the scores for pain and mobility results in an absolute estimation of hip function.

Countries

Norway

Outcome results

None listed

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