Now Available: Final Rule for FDAAA 801 and NIH Policy on Clinical Trial Reporting

Diffusion of Local Anesthetic After Median Nerve Block (Echoalr)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Hopital Foch
ClinicalTrials.gov Identifier:
NCT00651170
First received: March 28, 2008
Last updated: September 23, 2016
Last verified: September 2016
  Purpose
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..

Condition
Median Nerve

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Can Ultrasound Predict Success of Median Nerve Block? Relationship Between Diffusion of Local Anesthetic and Effectiveness of a Nerve Block

Resource links provided by NLM:


Further study details as provided by Hopital Foch:

Primary Outcome Measures:
  • Anesthesic diffusion degree [ Time Frame: 1 hour ] [ Designated as safety issue: No ]

Enrollment: 103
Study Start Date: March 2008
Study Completion Date: March 2009
Primary Completion Date: March 2009 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
primary care clinic
Criteria

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.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00651170

Locations
France
Hôpital Foch
Suresnes, France, 92151
Hôpital privé de l'Ouest Parisien
Trappes, France, 78195
Sponsors and Collaborators
Hopital Foch
Investigators
Study Chair: Marc Fischler Hopital Foch
  More Information

Responsible Party: Hopital Foch
ClinicalTrials.gov Identifier: NCT00651170     History of Changes
Other Study ID Numbers: 2008/01 
Study First Received: March 28, 2008
Last Updated: September 23, 2016
Health Authority: France: Ministry of Health
Individual Participant Data  
Plan to Share IPD: No

Keywords provided by Hopital Foch:
Median block nerve
Ultrasound

Additional relevant MeSH terms:
Anesthetics
Anesthetics, Local
Central Nervous System Depressants
Physiological Effects of Drugs
Sensory System Agents
Peripheral Nervous System Agents

ClinicalTrials.gov processed this record on December 07, 2016