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Weight Bearing Strategies for Post-Hip Arthroscopy Recovery

N/A
Waitlist Available
Research Sponsored by University of Pittsburgh
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6-week, 3 months, and 6-month post-operative
Awards & highlights

Study Summary

This trial looks at how soon after hip arthroscopic surgery patients can bear weight, to help them recover faster and get better outcomes.

Who is the study for?
This trial is for individuals aged 12 or older with hip impingement syndrome or a hip labral tear, who will undergo or have undergone hip arthroscopy with femoroplasty and labral repair at UPMC Children's or St. Margaret's Hospital. Both unilateral and bilateral cases are accepted. Those with musculoskeletal tumors, generalized hypermobility, or needing revision surgeries cannot participate.Check my eligibility
What is being tested?
The study compares two post-surgery approaches to weight bearing: 'Weight Bearing as Tolerated' (WBAT) allows patients to put as much weight on the foot as comfortable immediately after surgery; 'Flat Foot Weight Bearing' (FFWB) means only the sole of the foot may bear weight right away.See study design
What are the potential side effects?
While specific side effects aren't listed for these interventions, potential risks generally include discomfort while bearing weight, delayed healing if too much pressure is applied too soon, and possible complications leading to additional treatment.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6-week, 3 months, and 6-month post-operative
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6-week, 3 months, and 6-month post-operative for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Hip Outcome Score (HOS) ADL
Hip Outcome Score (HOS) Sport
Hip and Groin Outcome Score (HAGOS)
+2 more
Secondary outcome measures
Diagnostic ultrasound assessment of bilateral anterior hip capsule thickness
Diagnostic ultrasound assessment of incision widening
Diagnostic ultrasound for focal echogenic adhesions
+1 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Weight bearing as tolerated (WBAT) immediately following surgery.Experimental Treatment1 Intervention
Subjects will be able to self-select weight bearing based on pain and confidence in surgical hip.
Group II: Flat foot weight bearing (FFWB) for 2 weeks after surgery.Active Control1 Intervention
Subjects will be limited to FFWB, approx 20lbs through the surgical hip.

Find a Location

Who is running the clinical trial?

University of PittsburghLead Sponsor
1,719 Previous Clinical Trials
16,342,261 Total Patients Enrolled

Media Library

Flat foot weight bearing (FFWB) Clinical Trial Eligibility Overview. Trial Name: NCT05720806 — N/A
Hip Impingement Syndrome Research Study Groups: Weight bearing as tolerated (WBAT) immediately following surgery., Flat foot weight bearing (FFWB) for 2 weeks after surgery.
Hip Impingement Syndrome Clinical Trial 2023: Flat foot weight bearing (FFWB) Highlights & Side Effects. Trial Name: NCT05720806 — N/A
Flat foot weight bearing (FFWB) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05720806 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Does this research program admit participants aged 30 or older?

"According to the inclusion criteria, individuals aged 12 - 65 are eligible for this trial. There also exist separate trials specifically designed for participants under 18 and another one devoted solely to those over 65 years of age."

Answered by AI

Are there any present openings for the experiment?

"Per details posted on clinicaltrials.gov, this particular medical study is no longer recruiting participants - it was first announced March 10th 2023 and last updated February 7th 2023. Nonetheless, there are two other trials presently enrolling patients for the same type of research."

Answered by AI

Who meets the criteria necessary to be accepted into this experiment?

"This medical research is recruiting 80 participants aged between 12 and 65 years, who have been diagnosed with femoroacetabular impingement syndrome. It's mandatory that candidates must also have undergone a hip arthroscopy accompanied by femoroplasty and labral repair at either UPMC Children’s or UPMC St. Margaret’s Hospital for unilateral or bilateral hips respectively."

Answered by AI

What is the main goal of this experimental endeavor?

"This clinical trial has a 6-month follow-up period with the aim of assessing Hip and Groin Outcome Score (HAGOS). Additionally, ultrasound will be employed to gauge bilateral anterior hip capsule thickness, incision widening, and possible echogenic adhesions. Normal hip capsular thickness is estimated at 7-8 mm for healthy subjects while dysplastic hips usually range from 3.2 +/- 0.5mm and femoroacetabular impingement cases are 4.7 +/- 0.6 mm in thickness."

Answered by AI
~32 spots leftby Jan 2025