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Bone Forming at Prosthetic Surfaces. Fingerprint2

Bone Forming at Prosthetic Surfaces. A Randomized Clinical F-PET/CT Study

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01623687
Enrollment
26
Registered
2012-06-20
Start date
2011-08-31
Completion date
2015-03-31
Last updated
2014-04-04

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

Conditions

Osteo Arthritis

Keywords

total hip arthroplasty, bone metabolism, mineralisation

Brief summary

What is the intensity of F-PET uptake in healthy and osteo arthritic femur and acetabulum, compared to the uptake adjacent to four analyzed endoprosthetic components 1½ and 6 months after surgery?

Detailed description

A clinical study of 26 patients, age 50-69 years, healthy unless osteoarthritis in one hip, randomized in four groups plus a reference group of same 26 patient´s contralateral healthy hip. Intervention will be surgery with a total hip arthroplasty. The studied endoprosthetic components are: Cemented Lubinus SP II stem with a ceramic 32 mm head, a cemented Lubinus cross linked cup (Waldemar Link, Hamburg, Germany). Palacose cement with gentamycin, applied with 3:rd generation cementation technique will be used for those cemented implants. Uncemented HA-coated Corail stem with a ceramic 32 mm head (DePuy, Johnson & Johnson, USA), a fibrous metal Regenerex RingLoc cup (Biomet, Warsaw, Il, USA) All cups will have cross linked Ultra-high-molecular-weight polyethylene (UHWMP). Clinical score, radiography and PET uptake of Fluoride tracer (SUV) adjacent to the prosthetic surfaces will be analyzed.

Interventions

DEVICEComponent for acetabulum (Regenerex RingLoc cup)

A fibrous metal uncemented Regenerex RingLoc cup (Biomet, Warsaw, Il, USA)

DEVICEComponents for the acetabulum (Lubinus cross linked cup)

cemented Lubinus cross linked cup (Waldemar Link, Hamburg, Germany).

DEVICEArthroplasty components are for the femur (Cemented Lubinus SP II stem)

Cemented Lubinus SP II stem (Waldemar Link, Hamburg, Germany) with a ceramic 32 mm head.

DEVICEArthroplasty components are for the femur (Corail stem)

Uncemented HA-coated Corail stem with a ceramic 32 mm head (DePuy, Johnsson & Johnsson, USA).

Sponsors

Uppsala University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to 69 Years
Healthy volunteers
No

Inclusion criteria

* patients diagnosed to have unilateral hip osteo arthritis (Charnley group A) aimed for THA at the orthopedic clinic Gävle hospital.

Exclusion criteria

* Systemic disease or medication affecting the skeleton

Design outcomes

Primary

MeasureTime frameDescription
FEMUR: to analyze difference in SUV of the 4 upper ROI's (No 1, 7, 8 and 13) analyzed together between the cemented and uncemented groups AND: to analyze SUV of the 4 upper ROI's analyzed together between each femur study group and the reference group6 weeks after surgeryThere are two study groups for femur: cemented and uncemented femur prosthetic components. There are also a femur reference group.
ACETABULUM: to analyze difference in SUV of all 9 ROI's analyzed together between the cemented and uncemented acetabular study groups, and to analyze SUV of all 9 ROI's analyzed together between each acetabulum study group and the reference group6 weeks after surgeryThere are two study groups for acetabulum: cemented and uncemented acetabular prosthetic components. There are also an acetabular reference group.

Secondary

MeasureTime frame
FEMUR:to analyze difference in SUV for each individual ROI between the 3 time points for the cemented group. To analyze difference in SUV for each individual ROI between the 3 time points for the uncemented group.preoperatively, 6 weeks and 6 months
FEMUR:to analyze difference in SUV for the 4 upper ROI's (No 1, 7, 8 and 13)analyzed together between the 2 study groups6 months
FEMUR:to analyze difference in SUV for the 4 upper ROI's analyzed together between each study group and the reference group6 months
ACETABULUM: to analyze difference in SUV for each individual ROI between the 2 study groups6 weeks and 6 months
FEMUR:to analyze difference in SUV for each individual ROI inbetween the cemented and uncemented femur group6 weeks and 6 months
ACETABULUM: to analyze difference in SUV for each individual ROI for the cemented study group between the 3 time points. To analyze difference in SUV for each individual ROI for the uncemented study group between the 3 time points.preoperatively, 6 weeks and 6 months
ACETABULUM: to analyze difference in SUV of all 9 ROI's analyzed together between the cemented and uncemented acetabular study groups6 months
ACETABULUM: to analyze difference in SUV of all 9 ROI's analyzed together between the cemented and uncemented acetabular study groups, and to analyze SUV of all 9 ROI's analyzed together between each acetabulum study group and the reference group6 months
ACETABULUM: to analyze difference in SUV for each individual ROI between the cemented study group and the reference group. To analyze difference in SUV for each individual ROI between the uncemented study group and the reference group.6 weeks and 6 months
FEMUR: to analyze difference in SUV for each individual ROI between the cemented study group and the reference group. To analyze difference in SUV for each individual ROI between the uncemented study group and the reference group.6 weks and 6 months

Countries

Sweden

Contacts

Primary ContactGösta Ullmark, MD, PhD
gosta.ullmark@lg.se+46706466149

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026