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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
GroupInterventionDescription
2median nerve blockpatients without a carpal tunnel syndrome
1median nerve blockpatients with a carpal tunnel syndrome
Primary Outcome Measures
NameTimeMethod
light touch sensibility30 minutes following block performance
Secondary Outcome Measures
NameTimeMethod
ice touch sensibility30 minutes following block performance
motor block30 minutes following block performance
paresthesiaduring nerve block procedure
vascular punctureduring nerve block procedure

Trial Locations

Locations (2)

Hôpital Privé de l'Ouest Parisien

🇫🇷

Trappes, France

Hopital Foch

🇫🇷

Suresnes, France

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