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HIPAA Compliant
ISO 27001 Certified

Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05950022

Comparing Endoscopic Ilio-Psoas Tendon Release at Lesser Trochanter Versus Acetabular Notch for Hip Pain After Total Hip Replacement

Led by GCS Ramsay Santé pour l'Enseignement et la Recherche · Updated on 2026-04-01

108

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

G

GCS Ramsay Santé pour l'Enseignement et la Recherche

Lead Sponsor

E

Euraxi Pharma

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to compare two surgical techniques for treating iliopsoas tendinopathy caused by impingement between the iliopsoas tendon and the prosthetic cup in patients who have undergone total hip replacement. The study evaluates clinical improvement using the Oxford Hip Score measured at baseline, 2 months, and over 12 months after surgery. It is a randomized, single-blind, comparative trial conducted at a single center. Participants will undergo endoscopic tenotomy surgery of the iliopsoas tendon, performed either at the lesser trochanter or at the acetabular notch. Patients are randomly assigned to one of these two groups by drawing lots. The surgery is carried out under general anesthesia with standardized multimodal pain management, and all other surgical approaches and postoperative care remain consistent between groups. During the study, patients will be assessed with the Oxford Hip Score before surgery, at 2 months, and at more than 12 months after the procedure to measure clinical improvement. The study monitors patient outcomes and recovery following the surgery. Participation involves preoperative consultation, surgery, and follow-up assessments over at least one year to evaluate the treatment effect.

CONDITIONS

Brief Title

Clinical Improvement Obtained by Endoscopic Ilio-Psoas Tenotomy (Lesser Trochanter Versus Acetabular Notch)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Confirmed diagnosis of iliopsoas tendinopathy caused by conflict between the tendon and prosthetic cup
  • Failure of first-line conservative treatments
  • Planned for endoscopic tenotomy surgery
  • Affiliated with a social security scheme
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • Revision total hip prosthesis or multiple prior hip surgeries before tenotomy
  • Other surgical or medical interventions planned during the study
  • Participation in another clinical trial or within a restricted period from another trial
  • Pregnant, likely to be pregnant without effective contraception, or breastfeeding
  • Deprived of liberty, under guardianship or curatorship, or unable to give consent

Research Team

N

Nicolas BONIN, MD

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