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Osteoarthritis, Hip clinical trials

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NCT ID: NCT01700933 Completed - Osteoarthritis, Hip Clinical Trials

Dose-response: Exercise Therapy on Hip Osteoarthritis

Start date: September 2012
Phase: N/A
Study type: Interventional

Osteoarthritis is a common disease that causes muscle weakness, stiffness and instability. The disease reduces the opportunities for an active lifestyle. Exercise Therapy provides a well-documented effect on pain and function in patients with osteoarthritis of the hip. It is sought an optimal dose of exercise, in which this study will help to investigate. We hypothesize that an exercise program designed to have a high number of repetitions will benefit the outcome of the training in a more positive way than a low-repetition based program.

NCT ID: NCT01695213 Completed - Clinical trials for Patients With Osteoarthritis of the Hip Joint Elligable for a Uncemented Hipprosthesis

RCT Comparing the DEXA Results of the HA-Omnifit Versus the Symax Uncemented Hip Stem

Start date: April 2003
Phase: Phase 4
Study type: Interventional

Thr purpose of this study is to compare the clinical and radiological results, as well as the femur bone density measurements of two uncemented total hip prostheses during 5 years of follow up.

NCT ID: NCT01683955 Completed - Osteoarthritis, Hip Clinical Trials

Topical Tranexamic Acid and Acute Blood Loss in Total Hip Arthroplasty

Start date: January 1, 2013
Phase: Phase 1
Study type: Interventional

This study aims to assess postoperative blood loss and transfusion rates in total hip replacement after one-time administration of topical tranexamic acid.

NCT ID: NCT01668160 Withdrawn - Clinical trials for Osteoarthritis of Hip

Stability of Revision Total Hip Arthroplasty Implants Using Radiostereometric Analysis

Start date: February 2012
Phase: N/A
Study type: Interventional

The specific aim is to quantify the stability of the acetabular and femoral components of a revision total hip arthroplasty (THA) in vivo as currently performed at our institution. In this way, the investigators will gain insight into the outcome of the current state of the art of revision arthroplasty surgery. In the past, acetabular and femoral component stability has been measured using radiostereometric analysis (RSA) and when patients having revision total hip operations were compared to patients undergoing primary total hip operations it was possible to determine differences in stability and this was predictive of the intermediate to long-term performance of the acetabular and femoral reconstruction. The investigators propose to use this established, high resolution technique to assess and compare the stability of the revision implants.

NCT ID: NCT01636375 Completed - Osteoarthritis, Hip Clinical Trials

Comparison of Muscle Atrophy After Direct Anterior & Posterior Total Hip Arthroplasty

Start date: May 2012
Phase:
Study type: Observational

This project is designed to use MRI to evaluate pre- and post-arthroplasty hips; the specific aims of this project are three-fold. First, the investigators intend to compare the amount of muscle atrophy and tendon damage that occurs around the hip between two commonly-used operative approaches: the direct-anterior approach and the posterior approach. Second, the investigators aim to provide baseline data on the amount of muscle atrophy and tendon damage that should reasonably be expected to occur with both of these approaches. Third, the investigators will document the degree of recovery of the periprosthetic soft tissues post-surgery in both patient groups. The investigators first hypothesis is that the posterior approach will demonstrate significantly more damage to the abductors, piriformis, and short external rotators than the direct anterior approach, which will demonstrate minimal soft tissue damage. The investigators second hypothesis is that both surgical approaches will cause some degree of baseline muscle damage and atrophy, in a predictable pattern. The investigators third hypothesis is that each of the surgical approaches inherently cause some degree of soft tissue damage, and that the periprosthetic soft tissues that are incised during the surgical exposure will recover in a predictable pattern which is consistent but unique within each group

NCT ID: NCT01630941 Completed - Osteoarthritis, Hip Clinical Trials

Effects of Denosumab on Periprosthetic Bone After Total Hip Arthroplasty

Start date: August 7, 2012
Phase: Phase 2
Study type: Interventional

The primary objective is to study the effect of Denosumab on Bone Mineral Density, Standardised Uptake Value and bone metabolism in patients with total hip arthroplasty. The primary hypothesis is to demonstrate that Denosumab is superior to placebo.

NCT ID: NCT01622465 Completed - Osteoarthritis, Hip Clinical Trials

Effect of Cycle Ergometer in the Rehabilitation of Elderly Patients With Total Hip Arthroplasty

Start date: August 2011
Phase: Phase 2
Study type: Interventional

The aim of this study is to evaluate the effects of an exercise program with a cycle ergometer in functional outcome and related-health quality of life (RHQL) in elderly patients with total hip arthroplasty.

NCT ID: NCT01618708 Completed - Osteoarthritis, Hip Clinical Trials

A Study of the Safety and Effectiveness of Synvisc-One® (Hylan G-F 20) in Patients With Primary Osteoarthritis of the Hip

Start date: September 2012
Phase: N/A
Study type: Interventional

The primary objective of this study is to demonstrate any changes in assessments of pain for patients receiving Synvisc-One compared to control.

NCT ID: NCT01616667 Completed - Clinical trials for Unilateral Primary Osteoarthritis of Hip

Comparing the Clinical Effects of Posterior Approach Versus Lateral Approach in Osteoarthritis Patients With a THA

COMPALA
Start date: May 2012
Phase: Phase 2
Study type: Interventional

The aim of this study is to investigate the clinical outcome of the two different, but widely used, surgical approaches (Posterior approach and Lateral approach) of primary total hip arthroplasty in patients diagnosed with osteoarthritis. This study is divided into one main study and two sub-studies. The main study investigates the patient-reported outcome measures (questionnaire) within the first year post surgery. The two sub-studies investigate; i) the level of physical function and pain within the first 3 month after surgery, and ii) investigate the potential difference the two approaches have on gait-patterns and maximal isometric hip-muscle-strength, within the first year after surgery. Both approaches are described with potential drawbacks. Posterior approach has a higher risk of dislocation of the prostheses and revision due to dislocation compared with Lateral approach. Contrary, Lateral approach is described with the potential drawbacks of pain, lower physical function, gait abnormalities and muscle weakness, leading to less satisfied patients. However, according to a Cochrane analysis from 2004 concludes, more investigation is needed to determine the extent of differences.

NCT ID: NCT01583465 Completed - Clinical trials for Arthritis, Rheumatoid

Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermuscular Approach Total Hip Arthroplasty

Aquamantys
Start date: October 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to establish whether or not there is a clinical advantage to the use of Aquamantys® System from Medtronic Advanced Energy (formerly Salient Surgical Technologies) in patients undergoing primary total hip arthroplasty via the anterior supine intermuscular surgical approach in terms of blood loss, transfusion and wound healing. Wound healing will be assessed by a blinded observer and based upon a simple and subjective criteria: a) as expected, b) better than expected or c) worse than expected. The blinded observer is experienced in the care of the surgical patient and wound evaluation.