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Osteoarthritis, Hip clinical trials

View clinical trials related to Osteoarthritis, Hip.

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NCT ID: NCT03897595 Completed - Hip Osteoarthritis Clinical Trials

Assess the Mid-term Performance of the Mpact Cup in Subjects Requiring Total Hip Arthroplasty

Start date: October 2012
Phase:
Study type: Observational

Monitor the performance of the Mpact cup in the treatment of patients with hip joint disease requiring a total hip replacement.

NCT ID: NCT03891199 Completed - Surgery Clinical Trials

Two Year Study With Robotic-Arm Assisted Hip Surgery.

Start date: April 8, 2019
Phase: N/A
Study type: Interventional

This study will involve a quantitative assessment of prospectively collected computed tomography, radiographic and patient outcomes data from multiple centers. Specifically looking at acetabular cup placement during Total Hip Arthroplasty by either traditional or robotic-arm assisted placement.

NCT ID: NCT03875976 Completed - Hip Osteoarthritis Clinical Trials

Total Hip Arthroplasty: Fast Track Protocol is the Future?

FastTrack-H
Start date: March 1, 2018
Phase: N/A
Study type: Interventional

Fast-track total hip arthroplasty (THA) is a well-established concept including optimized logistics and evidence-based treatment, focusing on minimizing surgical stress and improved post-operative recovery. The aim of this protocol is to compare the standard care and fast track total hip arthroplasties in terms of functional and subjective outcomes, hospital staying, number of transfusions and analgesic consumption.

NCT ID: NCT03869229 Recruiting - Osteoarthritis Clinical Trials

Adipose-derived Mesenchymal Stem Cells in Osteoarthritis

Start date: April 5, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

This phase I/II study will enroll 100 subjects with mild to moderate osteoarthritis of the hip/knee/glenohumeral joints will be enrolled according to strict inclusion and exclusion criteria. Subjects will receive a single dose of at least 10 million of autologous Adipose-derived Mesenchymal Stem Cells (ADMCS) every three months for 12 months (maximum four doses in total and at least 40 million of ADMCS in total) via ultrasound guided intra-articular injection.

NCT ID: NCT03866330 Recruiting - Osteoarthritis Clinical Trials

Wharton's Jelly-derived Mesenchymal Stem Cells in Osteoarthritis

Start date: March 1, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

This phase I/II study will enroll 100 subjects with mild to moderate osteoarthritis of the hip/knee/ glenohumeral joint will be enrolled according to strict inclusion and exclusion criteria. Subjects will receive every three months a single dose of at least 10 million of Wharton Jelly derived Mesenchymal Stem Cells (WJMSC) form the Polish Stem Cell Bank for 12 months (maximum four doses in total and at least 40 million of WJMSC in total) via ultrasound guided intra-articular injection.

NCT ID: NCT03846791 Recruiting - Osteoarthritis, Hip Clinical Trials

An Evaluation of Health Outcomes for Mako Hip Replacement

HELLO
Start date: July 15, 2019
Phase:
Study type: Observational

To assess clinical outcomes and surgery related resource use in the year post surgery for patients undergoing hip replacement using the Mako Robo

NCT ID: NCT03846063 Completed - Osteoarthritis, Hip Clinical Trials

Development of an Effective Home-based-exercise-strategy

Start date: December 2015
Phase: N/A
Study type: Interventional

Osteoarthritis is one of the most common chronic diseases of the musculoskeletal system in elderly. Patients with osteoarthritis experience pain, stiffness and loss of mobility. Due to ageing Western societies in the coming decades the number of elderly with osteoarthritis will progressively increase. Osteoarthritis is a common indicator for a Total Hip Arthroplasty (THA). A hip replacement is one of the most successful orthopedic surgeries. However, with regard to the postoperative rehabilitation a lot can be improved. The current situation after a THA is that physical therapy in the Netherlands is not prescribed by default. Patients are resigned from the hospital and receive home exercises. However, it is not clear whether patients actually carry out these exercises and whether they perform the exercises correctly.

NCT ID: NCT03838874 Completed - Knee Osteoarthritis Clinical Trials

Mepivacaine Versus Low-Dose Bupivacaine For Primary Total Hip and Knee Arthroplasty

Start date: February 25, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

This research is being done to see if there is a difference between two different spinal anesthetics (Mepivacaine vs. Bupivacaine) as it relates to reducing post-operative complications and the time it takes for subjects to regain mobility after surgery.

NCT ID: NCT03809962 Recruiting - Coxarthrosis Clinical Trials

Efficacy and Safety of Ostenil® Plus in the Treatment of Coxarthrosis

Start date: January 30, 2019
Phase:
Study type: Observational

PMCF study to observe the Routine application of Ostenil® Plus in the Treatment of pain and restricted mobility in degenerative and traumatic changes of the Hip Joint.

NCT ID: NCT03803839 Completed - Hip Arthrosis Clinical Trials

Locally Administered Clodronate in the Prevention of Aseptic Implant Loosening

Start date: March 26, 2004
Phase: Early Phase 1
Study type: Interventional

Periprosthetic bone-loss after total hip arthroplasty (THA), detected as an early migration of the prosthesis, may predict later loosening. The investigators hypothesized that by reducing bone resorption after THA with bisphosphonates, it might be possible to achieve better early fixation of the implant. Nineteen patients suffering arthrosis were recruited to a prospective, double-blinded, randomized, placebo-controlled clinical pilot trial. Patients were operated with an uncemented Bimetric stem with tantalum markers, the acetabular cup and liner were chosen by the surgeon. The femoral proximal intramedullary canal was rinsed with 1mM (millimole) clodronate, that was done by adding the clodronate to the 1000 ml 0.9% NaCl (sodium chloride) in nine patients and rinsing solution was the pure 0.9% NaCl for 10 patients. These rinsing packages were labeled only with the code from the pharmacy of the hospital. These patients were followed for two years using radiostereometric analysis (RSA), dual energy x-ray absorptiometry (DXA) and the Harris hip score (HHS). The purpose of the investigator's study was to examine whether the local intraoperative administration of clodronate could reduce periprosthetic bone loss and further stem migration after primary THA.