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Active clinical trials for "Osteoarthritis, Hip"

Results 111-120 of 520

G7 Freedom Constrained Vivacit-E Liners

OsteoarthritisHip7 more

The main objectives of this study are to confirm the long-term safety, performance, and clinical benefits of the G7 Freedom Constrained Vivacit-E Acetabular Liners in primary and revision total hip arthroplasty.

Not yet recruiting26 enrollment criteria

Erector Spinae vs. Iliopsoas Plane Block for Total Hip Arthroplasty

Hip ArthropathyHip Osteoarthritis1 more

Effect of iliopsoas plane block and ESPB on pain management, and NLR and PLR following knee arthroplasty

Not yet recruiting2 enrollment criteria

Can Pre-operative Anemia be Timely Identified and Optimized in Patients Awaiting Primary Arthroplasty...

AnemiaHip Osteoarthritis

Reducing the occurrence of anemia (low circulating hemoglobin levels) post-surgery has been associated with improved outcome, as it reduces complications and allows for faster return to pre-operative function. Post-operative hemoglobin level is dependent upon its pre-operative value (for a given amount of blood loss). About 17% of patients at the Ottawa Hospital (TOH), will be anemic pre-operatively, and if left untreated the patients will have significantly inferior outcomes compared to non-anemic patients. In order to improve outcomes, when a patient is identified as anemic, typically at the pre-operative assessment clinic, he/she is invited to be reviewed and optimized at the Pre-operative Blood Optimization Clinic (PBOC). However, only a quarter of anemic patients are seen in the PBOC due to the lack of time available between anemia identification and surgery and the current resources available. This project will focus on hemoglobin level optimization of pre-operative hip and knee, primary, arthroplasty patients to demonstrate whether early assessment and treatment of pre-operative anemia can be successfully integrated into practice and its impact on post-operative outcomes. Patients will be randomly assigned to either the current standard of care pathway with an anemia test at the pre-operative assessment clinic (2-4 weeks before surgery), at which time they have the option to seek treatment. Patients who are randomly selected to be in the experimental group, will undergo a test to detect anemia at the time they consent for surgery, which is usually 4-6 months prior to surgery. Patients with anemia, will be invited for treatment at the blood optimization clinic at this time. In doing so, this project will test whether timely identification and simple measures is feasible and whether such practice can reduce the overall anemia burden and ultimately improve patient outcome.

Not yet recruiting5 enrollment criteria

Return to Golf After Orthopaedic Surgery

Hip OsteoarthritisKnee Osteoarthritis1 more

The GOLF study is a multicenter, prospective study with the goal to investigate golfers' return to the sport following hip, knee or shoulder arthroplasty. The prevalence of return to golf, by level of returning to golf will be assessed at 6 weeks, 3 months, 6 months, and 12 months postoperatively. Patients who are active golfers undergoing joint replacement will be identified from outpatient clinics and pre-assessment clinics and given information about the study at least two weeks prior to surgery. Participants in this study must have a desire to return to golf after surgery. Previous studies have only been able to report the return to golf after arthroplasty retrospectively; the prospective nature of this study will allow for a greater understanding of this process.

Recruiting8 enrollment criteria

Evaluating XPERIENCE™ Advanced Surgical Irrigation

Hip OsteoarthritisHip Arthritis2 more

A prospective, multi-center, double-arm, parallel, interventional, randomized, controlled clinical trial to assess the rate of periprosthetic joint infection (PJI) in patients undergoing primary total knee arthroplasty (TKA), total hip arthroplasty (THA) or hip resurfacing (HR) with XPERIENCE™ (XP) Advanced Surgical Irrigation versus dilute Betadine (DB).

Not yet recruiting19 enrollment criteria

Hip Prosthesis Components Position

Hip Arthrosis

The purpose of the study is

Not yet recruiting4 enrollment criteria

6-month Efficacy and Safety of Synolis VA 80/160 in Hip Osteoarthritis

OsteoarthritisHip

Multicenter, independent study of Synolis VA 80/160 over a period of 6 months

Not yet recruiting15 enrollment criteria

Comparison of Intra-articular Steroid Injection and Radiofrequency Thermocoagulation in Coxarthrosis...

Pain Hip Burning

The investigators aimed that the Comparison of effectiveness of the intra-articular steroid injection and radiofrequency thermocoagulation of the sensory branches of the femoral and obdurator nerves in coxarthrosis patients

Active10 enrollment criteria

RSA - ACTIS Hip Stem

Hip Osteoarthritis

The principal objective of this study is to compare mean 2-year subsidence of the ACTIS femoral stem using model-based RSA against published migration patterns for hip stems of a similar design. Secondary objectives include comparison of migration per surgical approach, quantifying changes in functional and health status of subjects following surgery, and assess occurrences of complications and adverse events.

Active14 enrollment criteria

A Prospective Multicenter Longitudinal Cohort Study of the Mymobility Platform

OsteoarthritisKnee2 more

Post-market prospective, multi-center longitudinal study to determine if mobile application-guided education and exercise paired with accurate and sensitive activity monitoring, captured from consumer wearables, can provide a viable (and potentially improved) alternative to current standard of care physical therapy for hip and knee arthroplasty.

Active13 enrollment criteria
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