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Clinical Trial Details — Status: Recruiting

Administrative data

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

Study information

Verified date June 2024
Source Rush University Medical Center
Contact Anne DeBenedetti, MSc
Phone 3124322468
Email anne.debenedetti@rushortho.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

This study examines the necessity of postoperative hip precautions in patients after primary total hip arthroplasty via the posterior approach. Precautions are instructions that limit the functional use of the hip and are given for the first six weeks after surgery, with the goal of preventing an instability event resulting in dislocation. The hip precautions that will be investigated in this study are: no hip flexion past 90ยบ, no crossing the legs, and no twisting at the waist.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Hip Precautions
Hip precautions are functional limitations of the hip replacement prescribed to patients for the first six weeks after surgery and are no hip flexion past 90º, no crossing the legs, and no twisting at the waist.
No Hip Precautions
Patients will not be prescribed hip precautions in the first 6 weeks after surgery. The hip precautions that will no longer be prescribed are: no hip flexion past 90º, no crossing the legs, and no twisting at the waist.

Locations

Country Name City State
United States Rush University Medical Center Chicago Illinois

Sponsors (1)

Lead Sponsor Collaborator
Rush University Medical Center

Country where clinical trial is conducted

United States, 

Outcome

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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