Tendinopathy
Conditions
Brief summary
The purpose of the study is to assess Oxford Hip Score at baseline, at 2 months and at over 12 months.
Detailed description
This is an interventional, comparative, randomized study, in 2 parallel groups, single-blind (the patient does not know which technique he will benefit from, the surgeon will carry out the surgery and will therefore be informed of the result of the randomization ) and monocentric. Comparative prospective cohort study of an endoscopic tenotomy surgery of the iliopsoas tendon at the level of the lesser trochanter versus at the level of the acetabular notch, in the context of anterior pain for impingement between the iliopsoas tendon and the prosthetic cup in patients after Total Hip Prosthesis. The study will be proposed to the patient during the preoperative consultation. Patients eligible for surgery will be offered the study. After a reflection period of at least 15 days, patients who agree to participate in the study will be included. Randomization will be done by drawing lots to decide whether the endoscopic tenotomy will be performed at the level of the lesser trochanter or at the level of the acetabular notch. The surgery will be performed under general anesthesia with standardized multimodal analgesia. Whatever the techniques, the approaches, the instruments to perform the procedure and the postoperative course will be identical, as in usual practice.
Interventions
PROCEDUREEndoscopic tenotomy surgery of the iliopsoas tendon
The surgery will be performed under general anesthesia with standardized multimodal analgesia. Whatever the techniques, the approaches, the instruments to perform the procedure and the postoperative course will be identical, as in usual practice.
Sponsors
GCS Ramsay Santé pour l'Enseignement et la Recherche
Euraxi Pharma
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Masking description
The patient does not know which technique he will benefit from, the surgeon will proceed with the surgery and will therefore be informed of the result of the randomization
Intervention model description
Interventional, comparative, randomized study, in 2 parallel groups, single-blind
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age ≥ 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.
Exclusion criteria
* Revision total hip prosthesis, multiple operations prior to tenotomy; * Other surgical or medical interventions planned during the study; * Participation in another clinical trial, or during a period of exclusion from another clinical trial; * Pregnant or likely to be pregnant (of childbearing age, without effective contraception) or breastfeeding; * Patient deprived of liberty or under guardianship or curatorship or unable to give consent.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Oxford Hip Score | 1 year | Compare the clinical improvement experienced by patients having an endoscopic tenotomy of the iliopsoas tendon at the level of the lesser trochanter versus at the level of the notch at more than 1 year minimum. The Oxford Hip Score is a self-administered patient-administered 12-item "Patient Reported Outcome Measures" questionnaire that allows the surgeon to assess clinical outcomes after total hip replacement. |
Countries
France
Contacts
CONTACTNicolas BONIN, MD
Outcome results
None listed