Efficacy of Median Nerve Block Performed Using Echographic Guidance
Completed
- Conditions
- Orthopedic
- Interventions
- Procedure: median nerve block
- Registration Number
- NCT00835653
- Lead Sponsor
- Hopital Foch
- Brief Summary
Observational study of the efficacy of median nerve blocks performed using echographic guidance in patients presenting with or without carpal tunnel syndrome.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
- short surgical procedure (less than 30 minutes) on the hand,
- regional anesthesia at the elbow involving the median nerve.
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Exclusion Criteria
- age less than 18 years,
- pregnant woman
- mental incapacity,
- poor understanding of French.
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Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description 2 median nerve block patients without a carpal tunnel syndrome 1 median nerve block patients with a carpal tunnel syndrome
- Primary Outcome Measures
Name Time Method light touch sensibility 30 minutes following block performance
- Secondary Outcome Measures
Name Time Method ice touch sensibility 30 minutes following block performance motor block 30 minutes following block performance paresthesia during nerve block procedure vascular puncture during nerve block procedure
Trial Locations
- Locations (2)
Hôpital Privé de l'Ouest Parisien
🇫🇷Trappes, France
Hopital Foch
🇫🇷Suresnes, France