Pharmacokinetic and Pharmacodynamic of Rocuronium
Information source: Pontificia Universidad Catolica de Chile
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Neuromuscular Blockade
Intervention: Rocuronium Bromide (Drug)
Phase: N/A
Status: Completed
Sponsored by: Pontificia Universidad Catolica de Chile Official(s) and/or principal investigator(s): Luis I Cortinez, MD, Study Chair, Affiliation: Ponticia Universidad Católica
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.
Clinical Details
Official title: Pharmacokinetic and Pharmacodynamic of Rocuronium Bromide Measured in Adductor Pollicis and Masseter Muscles.
Study design: Observational Model: Case-Only, Time Perspective: Prospective
Primary outcome: strength measuring 2 acceleromyograph. One Placed at the masseter muscle and the other one at the adductor pollicis muscle.Measure blood concentrations after administration rocuronium
Eligibility
Minimum age: 18 Years.
Maximum age: 65 Years.
Gender(s): Both.
Criteria:
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
Locations and Contacts
Additional Information
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Starting date: March 2013
Last updated: February 25, 2015
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