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Trials / Completed

CompletedNCT03545308

Pharmacokinetics of Rocuronium for Deep Block (DeepRocu)

Pharmacokinetics of Rocuronium (1 mg/kg) for Deep Block : a Prospective Observational Study

Status
Completed
Phase
Study type
Observational
Enrollment
250 (actual)
Sponsor
Centre Hospitalier Universitaire de Nīmes · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers

Summary

Rocuronium is a non-depolarising neuromuscular blocking agent. The compound has a rapid onset and an intermediate duration of action. The rapid onset is of importance in patients at risk for pulmonary aspiration, for elective induction of anesthesia. Clinical studies simulating rapid sequence induction in elective patients indicate that rocuronium 0.9 mg kg-1 may be suitable for crash intubation.Also, rocuronium may be an alternative to succinylcholine for rapid sequence induction when high dose is injected (3x Effective Dose 95 %= 1mg/kg). But, pharmacokinetic of rocuronium at 1 mg/kg is not well establish. The investigator investigate the onset and recovery of a single dose rocuronium (1 mg/kg) in consecutive patients (\>100) using adductor muscle monitoring (Train of Four and Post Tetanic Count)

Detailed description

In this study, pharmacokinetic of rocuronium at 1 mg/kg will be evaluated at each point of Train of Four Response (TOF) and Post Tetanic Count (when TOF=0) troughout the period of anesthesia and surgery. Time 0 is the time of rocuronium injection, Time 1 is the time when post tetanic count is \> 5-7 and TOF=0, Time 3 when TOF \>0 response, Time 4 when 4 reponses of the TOF and Time 5 when TOF \> 90 %

Conditions

Interventions

TypeNameDescription
DRUGRocuroniumDose: 1 mg/kg

Timeline

Start date
2017-08-25
Primary completion
2018-03-01
Completion
2018-03-01
First posted
2018-06-04
Last updated
2018-06-04

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT03545308. Inclusion in this directory is not an endorsement.