Osteoarthritis Clinical Trial
Official title:
Are Postoperative Hip Precautions Necessary After a Total Hip Arthroplasty Via the Posterior Approach: A Prospective Randomized Trial
NCT number | NCT02686528 |
Other study ID # | 13100906 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | January 2016 |
Est. completion date | September 2025 |
The purpose of this study is to determine if hip precautions, which are instructions that limit functional use of a hip replacement after surgery, affect the rate of dislocation in the first six weeks after primary total hip replacement surgery. The impact of hip precautions on a patient's return to activities of daily living and overall patient satisfaction will also be investigated. The overall cost effectiveness of hip precautions will be determined.
Status | Recruiting |
Enrollment | 1000 |
Est. completion date | September 2025 |
Est. primary completion date | January 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patients undergoing a primary total hip arthroplasty via the posterior approach by participating attending surgeons at this institution - Index diagnosis of noninflammatory arthritis - Patients must be able to understand and comply with study procedures Exclusion Criteria: - Allergy or intolerance to the study materials - History of previous surgeries on the affected joint other than arthroscopy; i.e. revision THA or open surgeries |
Country | Name | City | State |
---|---|---|---|
United States | Rush University Medical Center | Chicago | Illinois |
Lead Sponsor | Collaborator |
---|---|
Rush University Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Use of Assistive Devices After Surgery | Patients will be surveyed in clinic after surgery about their use of assistive devices including seat extenders, extra pillows between the legs, and walkers. The use of these devices between groups will be compared and the cost per patient in each group for use of these devices will be determined, allowing for analysis of potential cost savings for patients not prescribed hip precautions. | 6 months after surgery | |
Primary | Dislocation | Incidence of dislocation of the total hip arthroplasty will be recorded for both treatment groups. | 6 weeks after surgery | |
Secondary | Activities of Daily Living | The time from surgery to return to activities of daily living will be measured for both treatment groups. This includes return to activities of bathing, return to work, and return to driving. | 1 year after surgery |
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