NCT00651170

Brief Summary

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..

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
103

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Mar 2008

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2008

Completed
27 days until next milestone

First Submitted

Initial submission to the registry

March 28, 2008

Completed
5 days until next milestone

First Posted

Study publicly available on registry

April 2, 2008

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2009

Completed
Last Updated

September 26, 2016

Status Verified

September 1, 2016

Enrollment Period

1 year

First QC Date

March 28, 2008

Last Update Submit

September 23, 2016

Conditions

Median Nerve

Keywords

Median block nerveUltrasound

Outcome Measures

Primary Outcomes (1)

  • Anesthesic diffusion degree

    1 hour

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

primary care clinic

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Hôpital Foch

Suresnes, 92151, France

Location

Hôpital privé de l'Ouest Parisien

Trappes, 78195, France

Location

Study Officials

  • Marc Fischler

    Hopital Foch

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 28, 2008

First Posted

April 2, 2008

Study Start

March 1, 2008

Primary Completion

March 1, 2009

Study Completion

March 1, 2009

Last Updated

September 26, 2016

Record last verified: 2016-09

Data Sharing

IPD Sharing
Will not share

Locations

FR(2)