Diffusion of Local Anesthetic After Median Nerve Block

NCT ID: NCT00651170

Last Updated: 2016-09-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

103 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-03-31

Study Completion Date

2009-03-31

Brief Summary

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Median nerve block is widely practised, avoiding general anaesthesia in a number of cases and producing excellent post-operative analgesia in orthopedic surgery. Even realised by experienced anaesthetists,a failure rate of 5-15% is noticed. The principal aim of the study is to observe the local anesthetic solution diffusion after a conventional median nerve block technique using neurostimulation. The secondary objective is to compare diffusion and of block efficacy..

Detailed Description

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Conditions

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Median Nerve

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Patients undergoing elective hand surgery requiring a median block nerve.

Exclusion Criteria

* age lower than 18 years
* pregnancy
* contraindication to nerve block
* inability to read, write or speak French
* mental illness.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hopital Foch

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Marc Fischler

Role: STUDY_CHAIR

Hopital Foch

Locations

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Hôpital Foch

Suresnes, , France

Site Status

Hôpital privé de l'Ouest Parisien

Trappes, , France

Site Status

Countries

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France

Other Identifiers

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2008/01

Identifier Type: -

Identifier Source: org_study_id

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