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Osteoarthritis, Hip clinical trials

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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.

NCT ID: NCT01514318 Completed - Osteoarthritis, Hip Clinical Trials

Encore Revelation Hip Stem

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

The purpose of this study is to obtain long-term (10+ yrs) clinical and patient outcomes data on patients who received the Revelation Hip Stem prior to 2002.

NCT ID: NCT01506024 Completed - Hip Osteoarthritis Clinical Trials

Minimal Invasive Surgery in Total Hip Arthroplasty Patients; Short- and Long Term Results

Start date: September 2011
Phase: N/A
Study type: Interventional

The aim of the present study is to explore the most efficient surgical approach in total hip replacement in short and long term when concerning strength, functionality and postoperative complications. The objective is to register muscular strength, hip joint functionality/mobilisation and complications after total hip arthroplasty (THA) performed by the direct lateral approach (DLA), the posterior approach (PA) and the anterior approach (AA). The latter is a modified Smith-Petersen approach which follows the principles of minimally invasive surgery (MIS). The primary working hypothesis is that due to a minimal dissection and reduced trauma in the muscles, patients will tolerate early hospital discharge better after the AA than the PA and the DLA. Patients in the AA group are also thought to be more active and maintain muscular strength and hip joint functionality/mobilisation better than patients in the lateral group.

NCT ID: NCT01501955 Completed - Clinical trials for Osteoarthritis of the Hip

The Metaphyseal Hip Prosthesis - Total Hip

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

The purpose of this study is to analyze stability, safety and efficacy of the Metaphyseal Hip Prosthesis (MHP) compared to the Stanmore hip replacement.

NCT ID: NCT01500811 Completed - Hip Osteoarthritis Clinical Trials

Autologous Chondrocyte Intra-articular Implantation in Patients With Severe Hip Osteoarthritis

Start date: March 2011
Phase: Phase 1
Study type: Interventional

Hip osteoarthritis is degeneration of hip cartilage and inflammation of subchondral bone and soft tissue linings. Patients have pain, stiffness, swelling, and difficulty walking. There are treatments available to help manage these symptoms like weight loss, and analgesics. Surgery is the appropriate treatment in patients who have failed these conservative treatments. The aim of this clinical study is to assess safety of autologous cultured chondrocyte intra-articular injection and obtain its clinical results in patients with severe hip osteoarthritis.