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Pharmacokinetics of Rocuronium for Deep Block (DeepRocu)

C

Centre Hospitalier Universitaire de Nīmes

Status

Completed

Conditions

Neuromuscular Blockade

Treatments

Drug: Rocuronium

Study type

Observational

Funder types

Other

Identifiers

NCT03545308
2016-01-01

Details and patient eligibility

About

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)

Full 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 %

Enrollment

250 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • elective or emergency surgery under general anesthesia with deep block
  • approval
  • adult

Exclusion criteria

  • contra indication to neuromuscular blockade (allergy, myopathy, hyperkaliemia)
  • refusal
  • < 18 years olds
  • Body mass index > 50
  • neuropathy
  • regional anesthesia

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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