Actively Recruiting
Psoas Tenotomy Under Ultrasound for Ilio-Psoas Conflict After Total Hip Replacement
Led by Centre Hospitalier Universitaire de Nice · Updated on 2025-12-04
15
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate ultrasound-assisted psoas tenotomy in patients experiencing ilio-psoas conflict after total hip replacement. The ilio-psoas conflict is a common complication often related to mispositioning of the acetabular prosthetic component that irritates the ilio-psoas tendon. The study is designed to assess whether this ultrasound-guided procedure is feasible and how it impacts pain and functional outcomes compared to existing surgical methods. The procedure studied is a tenotomy of the ilio-psoas tendon performed under ultrasound guidance using a specific kit and a 3 mm Acufex hook blade. Patients will be under general anesthesia in a supine position with the hip extended 15 to 20 degrees. This approach aims to reduce scar tissue and simplify the surgical setup by avoiding more complex arthroscopic equipment. The study will not compare multiple groups but will focus on patients indicated for this tenotomy technique. Participants will be assessed for the success of the ultrasound-guided tenotomy three weeks after surgery, along with detailed pain evaluations at several points before and up to six months after the operation. Functional scores including the Oxford Hip Score, Harris Hip Score, and others will be measured at baseline and follow-up visits. Researchers will also monitor surgical parameters, complications, hospital stay length, scar healing, quality of life, patient satisfaction, and the need for rehabilitation over six months. Total participation will span at least six months post-surgery with multiple assessments to track outcomes and safety.
CONDITIONS
Brief Title
Psoas Tenotomy Under Ultrasound
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients 18 years of age or older
- Indication of psoas tenotomy for ilio-psoas conflict after total hip replacement
- Signed written informed consent form
- Affiliation to a French health insurance scheme or equivalent
You will not qualify if you...
- Pregnant or breastfeeding women
- Adults under guardianship or deprived of freedom
- Allergies to local anesthetics
- Patients on anticoagulant or antiplatelet agents
- Contraindication to surgery
- Refusal to participate in the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Day of surgery and the day after
Participants undergo psoas tenotomy under ultrasound, a procedure performed under general anesthesia. Immediate post-operative assessments include technical difficulty, operative time, installation time, blood loss, and length of hospital stay.
1 surgery visit and 1 post-operative visit (in-person)
Duration - 6 months post-operative
Participants are monitored for surgical complications, pain, hip function, scarring, quality of life, and patient satisfaction through several assessments over 6 months after surgery.
Visits at 3 hours, 1 day, 3 weeks, 6 weeks, 3 months, and 6 months post-operative (in-person and remote assessments)
Trial Site Locations
Total: 1 location
1
Nice University Hospital
Nice, Alpes Maritimes, France, 06000
Actively Recruiting
Research Team
G
Grégoire MICICOI
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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