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Coxarthrosis clinical trials

View clinical trials related to Coxarthrosis.

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NCT ID: NCT01046019 Completed - Coxarthrosis Clinical Trials

Measurement of Early Bone Loss Around a Total Hip Arthroplasty

DXACorail
Start date: September 2007
Phase: N/A
Study type: Observational

Research with DXA has shown the pattern of bone remodelling around an implant. The baseline and reference value for such calculations is the first measurement after the operation. The baseline measurement is performed at different time from study to study. If there is a rapid bone loss the first weeks after an operation, this will influence the reference value and then the results. To evaluate DXA as a method we decided to set up a study with 3 DXA measurements within the first 2 weeks. Our hypothesis is that there is a rapid bone loss the first 2 weeks after operation and that timing of the first post operative measurement will influence the later results.

NCT ID: NCT00317889 Completed - Coxarthrosis Clinical Trials

Compaction Total Hip Arthroplasty (THA) Bilateral

Start date: May 2001
Phase: N/A
Study type: Interventional

This is a prospective, randomized study comparing two different bone preparation techniques for insertion of a porous coated titanium cementless femoral stem. Patients receiving a bilateral total hip replacement are randomized to conventional broaching on one side and compaction on the other side. Hypothesis: Compaction results in significantly less stem migration [evaluated by radiostereometric analysis (RSA)], less peri-prosthetic bone mineral density (BMD) loss [evaluated by dual energy x-ray absorptiometry (DEXA)], and a higher Harris hip score after two years.

NCT ID: NCT00317863 Completed - Coxarthrosis Clinical Trials

Zink and Bone Strength

Start date: January 2004
Phase: N/A
Study type: Observational

Zink and bone strength

NCT ID: NCT00159497 Completed - Coxarthrosis Clinical Trials

Bone Remodeling Around HA-coated Acetabular Cups.

Start date: October 1998
Phase: Phase 4
Study type: Interventional

This study was designed to investigate the influence of HA-coating on bone remodeling around the cup in cementless THA. 100 patients gave informed consent to participate in a controlled randomized study between porous coated Trilogy® versus Trilogy Calcicoat®. The cup was inserted in press-fit fixation. The femoral component was a cementless porous coated titanium alloy stem (Bi-Metric®), with a modular 28 mm CrCo head. Effect parameters were Harris Hip Score (HHS) and Bone Mineral Density (BMD) determined by DEXA scanning. Measurements revealed no difference between the two groups after 3 years, neither in clinical outcome nor in terms of periprosthetic bone density. Patients with Body Mass Index above normal regained more bone mineral than patients with normal weight. This finding supports the assumption that load is beneficial to bone remodeling. Advantages of better sealing of the bone-prosthesis interface, preventing polyethylene induced osteolysis, may still be anticipated for the 7 or 12 year follow-up examinations