Pharmacokinetic and Pharmacodynamic of Rocuronium

Sponsor
Pontificia Universidad Catolica de Chile (Other)
Overall Status
Completed
CT.gov ID
NCT02376595
Collaborator
(none)
10
22

Study Details

Study Description

Brief Summary

The purpose of this study is characterize the dose-effect relationship of rocuronium bromide at the adductor pollicis and masseter muscles using an pharmacokinetic-pharmacodynamic (PKPD) model. The hypothesis is that masseter muscle has a greater sensitivity to the neuromuscular blockers (rocuronium), faster onset and slower recovery profile than the adductor pollicis muscle.

Condition or Disease Intervention/Treatment Phase
  • Drug: Rocuronium Bromide

Study Design

Study Type:
Observational
Actual Enrollment :
10 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Pharmacokinetic and Pharmacodynamic of Rocuronium Bromide Measured in Adductor Pollicis and Masseter Muscles.
Study Start Date :
Mar 1, 2013
Actual Primary Completion Date :
Nov 1, 2013
Actual Study Completion Date :
Jan 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Rocuronium Bromide

Rocuronium 0,3 mg/kg administered in less than five seconds, followed by a saline bolus.

Drug: Rocuronium Bromide
Rocuronium 0,3 mg/kg in less than five seconds, followed by a saline bolus.
Other Names:
  • Rocuronium Bromide Fresenius Kabi
  • Outcome Measures

    Primary Outcome Measures

    1. strength measuring 2 acceleromyograph. One Placed at the masseter muscle and the other one at the adductor pollicis muscle. [60 minutes]

    2. Measure blood concentrations after administration rocuronium [120 minutes]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Scheduled for elective surgery under general anesthesia.
    Exclusion Criteria:
    • Pregnancy.

    • Body mass index (BMI) >25 kg/m2.

    • Anticipated difficult airway.

    • Surgery associated with great volume loss.

    • Presence of any neuromuscular, hepatic, renal, cardiac or respiratory disease.

    • Previous history of neuromuscular blockade allergy, and/or administration of drugs known to interfere with neuromuscular blockade

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Pontificia Universidad Catolica de Chile

    Investigators

    • Study Chair: Luis I Cortinez, MD, Ponticia Universidad Católica

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Pontificia Universidad Catolica de Chile
    ClinicalTrials.gov Identifier:
    NCT02376595
    Other Study ID Numbers:
    • 12-003
    First Posted:
    Mar 3, 2015
    Last Update Posted:
    Mar 3, 2015
    Last Verified:
    Feb 1, 2015
    Keywords provided by Pontificia Universidad Catolica de Chile
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 3, 2015