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The Precision and Arm-to-Arm Variation of Mechanomyography and Acceleromyography for Monitoring of Neuromuscular Block

NCT00472121 · Status: COMPLETED · Type: OBSERVATIONAL

Last updated 2008-04-18

No results posted yet for this study

Summary

The purpose of the study is the examine the precision of acceleromyography and mechanomyography during recovery from a neuromuscular blocking agent and to examine whether there is any difference in monitoring block at the dominant or non-dominant arm. Our hypothesis is that there is no significant difference in neither the precision nor the level of block in the contralateral arms.

Conditions

  • Neuromuscular Blockade

Interventions

DEVICE

TOF-Watch SX (neuromuscular monitor)

The variation between arms (dominant or non-dominant) when monitored with the same method on both arms

Sponsors & Collaborators

  • Rigshospitalet, Denmark

    lead OTHER

Principal Investigators

  • Casper C Kjær, MD · Dep. of anaesthesia 4231, Rigshospitalet

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-05-31
Primary Completion
2007-10-31
Completion
2007-10-31

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00472121 on ClinicalTrials.gov