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Osteoarthritis of Hip clinical trials

View clinical trials related to Osteoarthritis of Hip.

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NCT ID: NCT04754087 Recruiting - Osteoarthritis, Hip Clinical Trials

G7 Acetabular System With Vivacit-E or Longevity Liner PMCF Study

Start date: July 7, 2021
Phase: N/A
Study type: Interventional

The main objectives of this study are to confirm the long-term safety, performance, and clinical benefits of the G7 Acetabular Shells when used with the Vivacit-E and Longevity HXLPE liners and instrumentation in primary and revision total hip arthroplasty.

NCT ID: NCT03966573 Completed - Quality of Life Clinical Trials

Femoral Lengthening Might Impair Physical Function and Lead to Structural Changes in Adjacent Joints

Start date: March 6, 2019
Phase: N/A
Study type: Interventional

This study evaluates function, quality of life and development of hip- and knee osteoarthritis minimum 15 years after unilateral femoral lengthening on people with idiopathic or post-traumatic anisomelia.

NCT ID: NCT03428893 Completed - Clinical trials for Osteoarthritis of Knee

Mobile Technology to Support Physical Therapy Exercise

MyTherEx
Start date: January 8, 2018
Phase: N/A
Study type: Interventional

Osteoarthritis is the leading cause of disability in the U.S, particularly in older adults. Exercise is an evidence-based treatment option that improves pain and disability outcomes in adults with osteoarthritis, but adherence to prescribed exercise is generally low. Technology such as mobile applications (apps) for smartphones and tablets offers the potential to support exercise adherence through evidence-based components and enhanced communication between physical therapists and patients. The investigators aim to test mobile app-supported physical therapy exercise prescription compared to standard care. The investigators propose to use a two-arm randomized control trial with subjects in the intervention receiving mobile app-supported physical therapy exercise prescription and the control group receiving usual care physical therapy exercise prescription (paper handouts and verbal instruction). No known studies have assessed the impact of technological integration on adherence with PT exercises for OA. Current approaches such as therapist drawn pictures, hand-written or print-ready instructions do not account for patient communication preferences or ability to translate drawings into physical action. Mobile technology offers a potential solution to patient-centered care but has not been evaluated. This study will provide valuable information on effectiveness and user perspectives to key stakeholders such as patients, health care administrators, physical therapists and app designers.

NCT ID: NCT03341442 Completed - Clinical trials for Osteoarthritis of Hip

A Study of Posterior Hip Precautions After Total Hip Arthroplasty

HIPPRECAU
Start date: April 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to perform a randomized controlled study to compare patients undergoing THA via a posterolateral approach to receive either standard of care post-surgery hip restrictions or to receive no restrictions. The investigators goal is to first complete a pilot study in which the investigators assess the short term dislocation rates 3-6 months and then continue to recruit into this study and follow these patients for a year to determine the 1 year risk for dislocation. The investigators also will compare the HOOS Jr. and VAS scores and time until free from walking aid. The research question is: Will the elimination of post operative posterior hip precautions increase the dislocation rate? The hypothesis is that the elimination of post operative hip precautions will not increase the dislocation rate.

NCT ID: NCT02836262 Recruiting - Clinical trials for Osteoarthritis of Hip

Hip Replacement System (HRS-P) in Primary Total Hip Arthroplasty

(HRS-P)
Start date: August 25, 2017
Phase: N/A
Study type: Interventional

To evaluate effectiveness and safety of HHRS in subjects undergoing total hip arthroplasty (THA). Effectiveness will be evaluated using patient-reported, clinical, radiologic, and radiostereometric outcomes. Safety will be evaluated through the collection of device-related and unanticipated device-related adverse events.

NCT ID: NCT02577822 Completed - Clinical trials for Osteoarthritis of Hip

The Viability of Short Stems in Total Hip Arthroplasty

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

The purpose of this study is to determine the viability of short femoral stems as an alternative to standard-length stems in total hip arthroplasty.

NCT ID: NCT02405104 Completed - Clinical trials for Osteoarthritis, Knee

Chlorzoxazone in Hip and Knee Arthroplasty

chlorzoxazon
Start date: September 1, 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to elucidate whether patients operated with THA and TKA can benefit from treatment with chlorzoxazone.

NCT ID: NCT02263209 Active, not recruiting - Clinical trials for Osteoarthritis of Hip

Investigation to Determine Safety of Taperloc Stems With BioGuard Coating When Used in Cementless Total Hip Arthroplasty

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

Prospective clinical investigation to determine the safety of Taperloc stems with BioGuard coating and Exceed ABT Taperfit acetabular cups with BioGuard coating when used in cementless total hip arthroplasty

NCT ID: NCT02162186 Completed - Avascular Necrosis Clinical Trials

Clinical and Radiographic Outcomes of the Corin Tri-Fit Total Hip Replacement

Start date: October 2014
Phase:
Study type: Observational

The study will evaluate the radiographs (x-rays) of 100 patients with a TriFIT total hip at 2 weeks, 3 months, 6 months, 12 months, and yearly following surgery to see if there has been any movement or wear in the hip stem over the course of the study. The study will also record clinical data on each patient using various functional tests and questionnaires at the same intervals.

NCT ID: NCT02161484 Terminated - Clinical trials for Total Hip Arthroplasty

Continuous Lumbar Plexus Block With and Without Parasacral Block in Patients Undergoing Total Hip Replacement

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

The purpose of this research study is to evaluate the analgesic efficacy of adding a single shot parasacral (sciatic) nerve block to a continuous lumbar plexus block in patients undergoing total hip replacement.