Status:
UNKNOWN
Evaluation of the Analgesic Efficiency of the Transcutaneous Neurostimulation in the Charcot Syndrome Marie Tooth on the Pains of Lower Limbs
Lead Sponsor:
Centre Hospitalier Universitaire de Nice
Conditions:
CHARCOT MARIE TOOTH DISEASE
Eligibility:
All Genders
18-75 years
Phase:
NA
Brief Summary
The Charcot syndrome Marie Tooth is the most frequent hereditary neuromuscular diseases: there is no curative treatment at present, on the other hand precautionary measures can be taken (physiotherapy...
Eligibility Criteria
Inclusion
- Age included between 18 and 75 years
- Affected by CMT confirmed on clinical, family criteria, electrophysiological and / or genetics
- pain ≥ 3 months
- EVA pain ≥ 4/10
- patient having given his written consent and lit(enlightened)
- patient susceptible to be followed regularly during at least 3 months
- Patient member to the Social Security
Exclusion
- Expanding patients of associated neurological pathology
- Patients having resorted to the TENS in the last 3 months
- Medical history of cancers, collagen and quite other pathology which can interfere with the experimental procedure
- Patient carrier of a pacemaker or an active implantable medical device
- Cutaneous hurt on the territory to be stimulated
- Venous or arterial thrombosis or thrombophlebitis in the territory to be stimulated
- Patient participant in another biomedical research on the pain or the period of exclusion of which in a study is not ended
- Patient under guardianship or deprived of all his liberties
Key Trial Info
Start Date :
June 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 1 2013
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT01918826
Start Date
June 1 2012
End Date
August 1 2013
Last Update
August 8 2013
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
CHU de Nice
Nice, France, 06000