Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06064136

Psoas Tenotomy Under Ultrasound

Led by Centre Hospitalier Universitaire de Nice · Updated on 2025-12-04

15

Participants Needed

1

Research Sites

39 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The ilio-psoas conflict is a commonly accepted complication after total hip replacement, often linked to a mispositioning of the acetabular prosthetic component that conflicts with the ilio-psoas tendon. To correct these pains, a psoas tenotomy can be proposed. The results proven by the literature are very satisfactory. Psoas tenotomy is performed endoscopically, arthroscopically, or more rarely open. The contribution of echo surgery allows to limit the scar ransom but also to free itself from a complex infrastructure to the operating room including an arthroscopy column and an intraoperative fluoroscopy for a conventional tenotomy, This also saves procedural and installation time. No studies to date have described ultrasound-assisted psoas tenotomy Yhe investigators conducted a cadaveric study of the feasibility of psoas tenotomy under ultrasound that confirms the feasibility of this technique and the safety of the gesture for the surrounding anatomical structures. The objectives of this study are to assess the feasibility, pain and functional outcomes of ultrasound-assisted psoas tenotomy in patients with ilio-psoas conflict after total hip replacement.

CONDITIONS

Official Title

Psoas Tenotomy Under Ultrasound

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 18 years of age or older
  • Indication of psoas tenotomy for ilio-psoas conflict after total hip replacement
  • Signature of the written informed consent form by the patient
  • Affiliation to a French health insurance scheme or equivalent
Not Eligible

You will not qualify if you...

  • Pregnant or breast-feeding women
  • Adults under guardianship or deprived of freedom
  • Allergies to local anesthetics
  • Patients on anticoagulant or antiplatelet agents
  • Contraindication to surgery
  • Refusal of patient involvement

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Nice University Hospital

Nice, Alpes Maritimes, France, 06000

Actively Recruiting

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Research Team

G

Grégoire MICICOI

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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