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Diffusion of Local Anesthetic After Median Nerve Block (Echoalr)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00651170
First Posted: April 2, 2008
Last Update Posted: September 26, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Hopital Foch
March 28, 2008
April 2, 2008
September 26, 2016
March 2008
March 2009   (Final data collection date for primary outcome measure)
Anesthesic diffusion degree [ Time Frame: 1 hour ]
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Complete list of historical versions of study NCT00651170 on ClinicalTrials.gov Archive Site
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Diffusion of Local Anesthetic After Median Nerve Block
Can Ultrasound Predict Success of Median Nerve Block? Relationship Between Diffusion of Local Anesthetic and Effectiveness of a Nerve Block
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..
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Observational
Observational Model: Cohort
Time Perspective: Prospective
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Probability Sample
primary care clinic
Median Nerve
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
103
March 2009
March 2009   (Final data collection date for primary outcome measure)

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.
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
France
 
 
NCT00651170
2008/01
No
Not Provided
Plan to Share IPD: No
Hopital Foch
Hopital Foch
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Study Chair: Marc Fischler Hopital Foch
Hopital Foch
September 2016