Carpal Tunnel Syndrome
Conditions
Brief summary
The objective of the study is to evaluate in patients suffering from carpal tunnel syndrome resistant to medical treatment, clinical course after percutaneous treatment under ultrasound guidance. 40 patients will be included in the study. The following parameters will be evaluated: patient satisfaction, pain, functional disability, quality of life and time to return to work. The medico-economic aspect will be analyzed.
Detailed description
Ultrasound analysis of Carpal tunnel is used for many years, especially for diagnostic purposes. Investigators have shown, first by a study of 104 cadavers that it was possible to reduce the opening by making the gesture under ultrasound guidance and to perform the procedure under local anesthesia. Then investigators performed an open study of 25 patients confirming the absence of iatrogenic lesions with this new technique. The percutaneous treatment of carpal tunnel syndrome under ultrasound guidance is a gesture of interventional radiology. One can envisage making this type of treatment in interventional radiology room which overcomes the operating room and thus reduce costs. The objective of the study is to continue the study of percutaneous treatment of carpal tunnel syndrome under ultrasound guidance by an open study conducted in interventional radiology room.
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
* Patient older than 18 years who signed the informed consent. * Patient with an Carpal Tunnel Syndrome
Exclusion criteria
* patient has already undergone surgery of Carpal Tunnel Syndrome * Patient with contra-indications to anesthesia (heart failure, kidney, liver). * Pregnant women * alcoholics in weaning period * Patient whose consent is altered or unable to get a safety procedure * Patient with contra-indication to lidocaine * Patient with contra-indication for the realization of ultrasound endoscopy (carpal tunnel syndrome secondary or anastomosis between the median and ulnar nerves: anastomosis Berritini)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pain (visual analogic scale) | change between baseline and day 90 after surgery | visual analogic scale |
| paresthesia | change between baseline and day 90 after surgery | — |
| muscle strength (dynamometer JAMARD) | change between baseline and day 90 after surgery | dynamometer JAMARD |
Countries
France