Actively Recruiting
Clinical Improvement Obtained by Endoscopic Ilio-Psoas Tenotomy (Lesser Trochanter Versus Acetabular Notch)
Led by GCS Ramsay Santé pour l'Enseignement et la Recherche · Updated on 2026-04-01
108
Participants Needed
1
Research Sites
258 weeks
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
The purpose of the study is to assess Oxford Hip Score at baseline, at 2 months and at over 12 months.
CONDITIONS
Official Title
Clinical Improvement Obtained by Endoscopic Ilio-Psoas Tenotomy (Lesser Trochanter Versus Acetabular Notch)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age �3e= 18 years old
- Definite diagnosis of iliopsoas tendinopathy due to conflict between the tendon and the prosthetic cup
- Failure of first-line conservative treatment
- Planned endoscopic tenotomy
- Affiliation to the social security scheme
- Signed informed consent
You will not qualify if you...
- Revision total hip prosthesis or multiple operations prior to tenotomy
- Other surgical or medical interventions planned during the study
- Participation in another clinical trial or exclusion period from another clinical trial
- Pregnant, likely to be pregnant without effective contraception, or breastfeeding
- Patient deprived of liberty or under guardianship, curatorship, or unable to give consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Clinique de la Sauvegarde
Lyon, France, 69009
Actively Recruiting
Research Team
N
Nicolas BONIN, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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