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Pharmacokinetic and Pharmacodynamic of Rocuronium

Pharmacokinetic and Pharmacodynamic of Rocuronium Bromide Measured in Adductor Pollicis and Masseter Muscles.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02376595
Enrollment
10
Registered
2015-03-03
Start date
2013-03-31
Completion date
2015-01-31
Last updated
2015-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neuromuscular Blockade

Keywords

Rocuronium, Pharmacokinetics, Pharmacodynamics

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.

Interventions

DRUGRocuronium Bromide

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

Sponsors

Pontificia Universidad Catolica de Chile
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
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

Design outcomes

Primary

MeasureTime frame
strength measuring 2 acceleromyograph. One Placed at the masseter muscle and the other one at the adductor pollicis muscle.60 minutes
Measure blood concentrations after administration rocuronium120 minutes

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026