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Hip Replacement clinical trials

View clinical trials related to Hip Replacement.

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NCT ID: NCT04886570 Not yet recruiting - Hip Arthropathy Clinical Trials

Clinical Follow-up of Hip Arthroplasty: A Cross-section and Longitudinal Study

Start date: June 1, 2021
Phase:
Study type: Observational

This longitudinal follow-up study aims to analyze how surgical and patient characteristics affect clinical outcomes in the subjects received total hip arthroplasty (THA) or hemiarthroplasty (HA).

NCT ID: NCT04322916 Active, not recruiting - Arthropathy of Hip Clinical Trials

Clinical Study With the RM Pressfit Vitamys Cup in Combination With a Mathys Stem

Start date: September 15, 2009
Phase:
Study type: Observational

The purpose of the study is the evaluation of the clinical and radiological short- to long-term safety and performance of the RM Pressfit vitamys cup. The data will be used for an ongoing evaluation of the product safety and performance.

NCT ID: NCT04199377 Recruiting - HIP REPLACEMENT Clinical Trials

Retrospective Evaluation of Clinical and Functional Results and Survivorship of Total Knee Replacement and Total Hip Replacement, Both Isolated or Combined.

ALLCCP
Start date: October 20, 2017
Phase: N/A
Study type: Interventional

Retrospective evaluation of clinical and functional results and survivorship of total knee replacement and total hip replacement, both isolated or combined.

NCT ID: NCT03610789 Enrolling by invitation - Hip Replacement Clinical Trials

A Multicenter, Post-Market Clinical Follow-up Study of Subjects With the REDAPTâ„¢ System Monolithic Sleeveless/Sleeved Stem and/or Fully Porous Acetabular Shell With XLPE Liner and/or Modular Shell Components Previously Implanted

Start date: May 7, 2018
Phase:
Study type: Observational

The primary purpose of this study is to demonstrate cumulative revision rate of the REDAPT System Monolithic Sleeveless/Sleeved Stem, Fully Porous Acetabular Shell with XLPE liner, and Modular Shell Components (with or without Staple, Slice and Blade Augments) at 10 years.

NCT ID: NCT03551860 Recruiting - Hip Replacement Clinical Trials

Quadratus Lumborum Block Versus Fascia Iliaca Nerve Block for Patients Undergoing Total Hip Replacement

Start date: April 10, 2018
Phase: N/A
Study type: Interventional

Investigators hypothesise that for patients undergoing elective total hip replacements, a single injection Transmuscular Quadratus Lumborum (TQL) block, when compared to a single injection Fascia Iliaca Block (FIB), will provide better analgesia and less motor block in the initial 24 hour period.

NCT ID: NCT03253419 Withdrawn - Hip Replacement Clinical Trials

HotShOT: Home Safety Occupational Therapy

HotShOT
Start date: August 15, 2017
Phase: N/A
Study type: Interventional

The purpose of this research study is to examine home safety and fall risk for patients who have undergone hip replacement surgery. The investigators want to know whether evaluating home safety impacts perceived and real risk of falls at home. The study will utilize a fall risk assessment which is a questionnaire that focuses on perceived and real risk of falls at home, as well as a home safety assessment application, the Home for Life App. The participant will be asked about the home environment, including areas of the home such as the entrance, bedroom, and bathroom, and modification recommendations will be made to potentially increase safety.

NCT ID: NCT03019198 Completed - Clinical trials for Blood Loss, Surgical

TRANEXAMIC ACID IN PATIENTS UNDERGOING TOTAL HIP ARTHROPLASTY IN A BRAZILIAN REFERENCE ORTHOPEDIC CENTER: A RANDOMIZED CONTROLLED TRIAL

Start date: December 2013
Phase: Phase 4
Study type: Interventional

This study aims to analyze the efficacy of intravenous tranexamic acid (TXA) in patients undergoing total hip arthroplasty (THA).

NCT ID: NCT02920151 Completed - Postural Balance Clinical Trials

Effects of Balance Exercises Circuit in Patients With Hip or Knee Arthroplasty

BECA
Start date: February 2015
Phase: N/A
Study type: Interventional

This study evaluates the effect of balance circuit in patients with more than one year of postoperative total hip or knee arthroplasty. Patients were randomized between intervention group (IG) (balance exercise circuit ) and control group (CG) (usual routine). The evaluations were conducted by blind examiners.

NCT ID: NCT02904681 Completed - Hip Replacement Clinical Trials

Multicenter Retrospective Evaluation of the Surgical Management of Spinal Growth Dystrophy

DRC
Start date: December 1, 2014
Phase: N/A
Study type: Observational

Spinal growth dystrophy (CRD), also called Scheuermann's disease, corresponding to impaired vertebral structure occurring in children and adolescents with involvement of the growth cartilage causing impaired growth and kyphosis. There are forms thoracolumbar and thoracic conventional forms of DRC with variable clinical expressions; the most important being kyphosis with spinal stiffness associated with painful elements. The radiographic definition according Sorenson is uniformisation 5 ° affecting at least three adjacent vertebrae. Scheuermann's disease and three problems. First, the thoracic kyphosis generates back pain which may be thoracic or lumbar indirectly attributed to compensatory lordosis. Moreover disruption sagittal balance frequently causes a significant aesthetic discomfort. Finally, scalability because the curvature may increase the likelihood of degenerative lesions disc degeneration or lumbar spinal stenosis for example. When the disease is diagnosed early, treatment is most often associated with orthopedic physiotherapy. However, for patients with active deformation, despite an orthopedic brace treatment with chronic pain, neurological deficit or for aesthetic reasons, surgical decision can be taken. The goal of surgical treatment of DRC is a correction of the thoracic kyphosis. It goes through a spinal fusion must be released from his column stiffness in a bad position, changing the equilibrium profile and ensure that it remains in a good position. This surgery usually requires a prior operative time (thoracic surgery to remove the intervertebral discs) and a posterior surgical time (blockage of the vertebrae together with a bone graft and osteosynthesis). Currently different surgical strategies are practiced there is no real consensus between the teams.

NCT ID: NCT02707302 Completed - Hip Replacement Clinical Trials

Surgical Adhesive Drapes for Prevention and Healing of Wound Infections After Total Hip Arthroplasty

Start date: January 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to support the rational use of iodophor-impregnated surgical adhesive drapes for preventing wound infections after total hip arthroplasty.