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Influence of a Single Dose Dexamethasone on the Time Course of Neuromuscular Blockade of Rocuronium

NCT01782820 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 108

Last updated 2022-08-17

No results posted yet for this study

Summary

The aim of the present study is to compare the time course of a neuromuscular block in patients receiving dexamethasone 8 mg in order to reduce postoperative nausea or vomiting several hours before surgery with patients receiving the drug immediately before induction of anaesthesia and patients without a dexamethasone prophylaxis. The primary end point is the time from start of injection of rocuronium until recovery to a train of four ratio (TOF ratio) of 0.9.

Conditions

  • Neuromuscular Block, Dexamethasone
  • Neuromuscular Block, Recovery

Sponsors & Collaborators

  • Kreiskrankenhaus Dormagen

    lead OTHER

Eligibility

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

Timeline & Regulatory

Start
2011-12-31
Primary Completion
2013-01-31
Completion
2013-01-31

Countries

  • Germany

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 NCT01782820 on ClinicalTrials.gov