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Osteoarthritis, Hip clinical trials

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NCT ID: NCT02102334 Completed - Clinical trials for Osteoarthritis of the Hip

Validity, Reliability and Reproducibility of Plain Radiographic Measurements After Total Hip Arthroplasty

Start date: September 2010
Phase: N/A
Study type: Observational

In total hip arthroplasty (THA), radiographic preoperative planning and postoperative evaluation of acetabular component, femoral offset (FO) and leg length discrepancy (LLD) require good validity, interobserver reliability and intraobserver reproducibility. Questions/purposes: (1) Evaluate the validity of the Sundsvall method of FO measurement by comparing it to a standard FO measurement method. (2) Evaluate the interobserver reliability and intraobserver reproducibility of measurement of FO, LLD, acetabular cup inclination and anteversion. 90 patients with primary unilateral osteoarthritis (OA) were included in this prospective study. On postoperative radiographs FO by the Sundsvall method, FO by a standard method, LLD, acetabular cup inclination and anteversion were measured. The interobserver reliability and intraobserver reproducibility were made by three independent observers. The validity and degree of prediction of Sundsvall method are measured by comparing its results with the standard method.

NCT ID: NCT02096211 Active, not recruiting - Osteoarthritis Clinical Trials

Ceramic-on-Ceramic (COC) 36mm Acetabular Bearing Insert Post Approval Study-New Subjects (COC36mmPAS)

COC36mmPAS
Start date: June 1, 2014
Phase:
Study type: Observational

This study is intended to gather short (Pre-operative to 4-years) and mid-term (5-years) information regarding the performance and safety of the commercially available 36mm CERAMAX® Ceramic on Ceramic Total Hip System from a cohort of new study subjects that were not previously involved in the IDE study for this device.

NCT ID: NCT02096198 Completed - Osteoarthritis Clinical Trials

Ceramic On Ceramic (COC) 36mm PAS IDE Rollover Subjects; Ceramic Acetabular Bearing With Ceramic Femoral Head in Total Hip Replacement

COC36mmPAS
Start date: January 1, 2014
Phase:
Study type: Observational

This study is intended to gather medium (5- to 7-years) and long-term (minimum 8- to 10-years) information regarding the performance and safety of the commercially available 36mm CERAMAX® Ceramic on Ceramic (COC) Total Hip System from a cohort of study subjects that were previously enrolled in the IDE study. (COC = 36mm ceramic acetabular bearing insert component that articulates with a ceramic femoral head in the COC total hip replacement system)

NCT ID: NCT02095093 Recruiting - Hip Osteoarthritis Clinical Trials

An Intelligent Instrument for Improved Leg Length and Hip Offset Accuracy in Total Hip Arthroplasty

Start date: March 2014
Phase: N/A
Study type: Interventional

Leg length discrepancies following total hip arthroplasty have been associated with nerve palsies, gait abnormalities, and lower back pain. Leg length discrepancies are related to poorer functional outcomes and patient dissatisfaction. Failure to restore femoral offset following total hip arthroplasty has been linked to decreased range of motion and abductor muscle strength, impingement, limping, higher dislocation rates, increased polyethylene wear, and loosening of implants. Computer navigation has shown to improve the accuracy of leg length and hip offset during total hip arthroplasty. The investigators research objective is to prove the accuracy of the Intellijoint HIP™ system for determining leg length and hip offset. The investigators hypothesis was that Intellijoint HIP™, an imageless intraoperative intelligent instrument, could improve the accuracy of leg length and hip offset during primary total hip arthroplasty. The investigators plan to study this hypothesis in humans by comparing the leg length and hip offset discrepancies produced with Intellijoint HIP™ to the standard at the investigators institution, which is a pin and outrigger system.

NCT ID: NCT02086474 Completed - Hip Osteoarthritis Clinical Trials

Daily Activity and Gait Analysis After Viscosupplement Injection Among Hip Osteoarthritis Patients

Start date: May 2014
Phase: Phase 4
Study type: Interventional

The objective of this study is to assess the changes in daily physical activity and gait pattern, following a viscosupplement injection among a population who is suffering from hip osteoarthritis. A kinetic and kinematic gait analysis, an Actigraph activity monitor, a functional Timed-Stair-Test and two questionnaires (Medical Outcome Study Short-Form36 (MOS-SF36), Hip disability and Osteoarthritis Outcome Score (HOOS)) about how the pathology affects the quality of life, will be use.

NCT ID: NCT02085824 Recruiting - Hip Osteoarthritis Clinical Trials

Comparison of Blood Loss Following Total Hip Arthroplasty With the Use of Three Thromboprophylactic Regimes: Dabigatran, Enoxaparin and Rivaroxaban.

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

The purpose of this study is to determine which of the following drugs: enoxaparin, dabigatran and rivaroxaban causes least blood loss after total hip replacement (THR).

NCT ID: NCT02079467 Recruiting - Osteoarthritis, Hip Clinical Trials

Unrestricted Rehabilitation Following Primary THA

Start date: December 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the form of rehabilitation following primary total hip arthroplasty has an influence on patient satisfaction or functional performance in the eighteen weeks following surgery.

NCT ID: NCT02062450 Completed - Femur Head Necrosis Clinical Trials

Observational Study Evaluating Outcomes of Hip Arthroplasty Using Tornier Dual Mobility Acetabular Cup

Start date: May 2013
Phase: N/A
Study type: Observational

The purpose of this study is to demonstrate the performance and reliability of Tornier "Dual Mobility Cup" used during primary total hip replacement or hip replacement revision surgery at least 24 months post-insertion.

NCT ID: NCT02047292 Completed - Hip Osteoarthritis Clinical Trials

Dynamic ROM Via Gait Analysis and 3D Fluoroscopy in THA With Different Head Diameters

DROMDP
Start date: January 2014
Phase: N/A
Study type: Interventional

Pain and reduced function are the most common symptoms of coxarthritis. Pain relief and normal range of motion (ROM) restoration are the objectives of a Total Hip Arthroplasty (THA) procedure. It is recognized that increased head-neck ratio results in increased ROM due to the fact that prosthetic impingement between neck and acetabular liner occurs with wider arcs of motion. This head-neck ratio has been investigated extensively only in vitro (on cadavers or sawbones) or using mathematical modeling in computer simulations. These studies are limited by the lack of soft tissues and muscle activations in the models. This study will clinically assess the effect of prosthetic head diameter on patient capability of performing movements which require extreme arcs of motion of the hip joint. Therefore, the research questions are: - What role do soft tissues play in limiting ROM? - Can prosthetic impingement really occur in a well positioned THA? - Can a bigger head diameter alone reduce the risk of impingement?

NCT ID: NCT02043613 Completed - Clinical trials for Osteoarthritis, Knee

Context Effects in Exercise Therapy for Knee and/or Hip Pain

CONEX
Start date: February 2014
Phase: N/A
Study type: Interventional

The study is designed to investigate the effect of physical surroundings on the effect of exercise therapy for knee and hip pain.