Efficacy of Median Nerve Block Performed Using Echographic Guidance

This study has been completed.
Sponsor:
Information provided by:
Hopital Foch
ClinicalTrials.gov Identifier:
NCT00835653
First received: February 2, 2009
Last updated: May 27, 2009
Last verified: May 2009

February 2, 2009
May 27, 2009
January 2009
May 2009   (final data collection date for primary outcome measure)
light touch sensibility [ Time Frame: 30 minutes following block performance ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00835653 on ClinicalTrials.gov Archive Site
  • ice touch sensibility [ Time Frame: 30 minutes following block performance ] [ Designated as safety issue: No ]
  • motor block [ Time Frame: 30 minutes following block performance ] [ Designated as safety issue: No ]
  • paresthesia [ Time Frame: during nerve block procedure ] [ Designated as safety issue: Yes ]
  • vascular puncture [ Time Frame: during nerve block procedure ] [ Designated as safety issue: Yes ]
Same as current
Not Provided
Not Provided
 
Efficacy of Median Nerve Block Performed Using Echographic Guidance
Efficacy of Median Nerve Block Performed Using Echographic Guidance

Observational study of the efficacy of median nerve blocks performed using echographic guidance in patients presenting with or without carpal tunnel syndrome.

Not Provided
Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample

patients scheduled for hand surgery

Orthopedic
Procedure: median nerve block
median nerve block performed under echographic guidance
  • 1
    patients with a carpal tunnel syndrome
    Intervention: Procedure: median nerve block
  • 2
    patients without a carpal tunnel syndrome
    Intervention: Procedure: median nerve block
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
70
May 2009
May 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • short surgical procedure (less than 30 minutes) on the hand,
  • regional anesthesia at the elbow involving the median nerve.

Exclusion Criteria:

  • age less than 18 years,
  • pregnant woman
  • mental incapacity,
  • poor understanding of French.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
France
 
NCT00835653
2008/42
No
Hopital Foch
Hopital Foch
Not Provided
Study Chair: Marc Fischler, MD Hopital Foch
Hopital Foch
May 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP