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A study comparing the effect of priming of rocuronium on the speed and ease of intubation in adult patients.

A Randomised trial to compare the onset time and intubating conditions using Rocuronium with or without priming in adult patients. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099243
Enrollment
100
Registered
2025-12-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: priming with rocuronium: the priming dose of rocuronium bromide 0.06 mg/kg (10% of intubating dose) will be given 3 min before the intubating dose followed by 0.54mg/kg intubating dose.

Sponsors

Government of Gujarat
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patients willing to consent for the study. 2)American Society of Anesthesiologist (ASA) Classification I, II, III

Exclusion criteria

Exclusion criteria: 1)Patients with neuromuscular diseases 2)anticipated difficult intubation (obesity, thyromental distance more than 6 cm and Mallampati grade 3 and 4) 3)pregnancy 4)hepatic, renal diseases 5)patients receiving drugs interfering with neuromuscular action 6) Patient refusal 7)ASA IV and V

Design outcomes

Primary

MeasureTime frame
To compare onset time of intubation and intubating conditions using Cooper Scoring system.Timepoint: Time interval between the intubating dose and the loss of T1 of TOF stimuli will be considered as onset time of intubation.—

Secondary

MeasureTime frame
To compare hemodynamic parameters and complicationsTimepoint: duration of surgery—

Countries

India

Contacts

Public ContactDr SMITA R ENGINEER

B.J. MEDICAL COLLEGE AND CIVIL HOSPITAL

seng_90@yahoo.com9825504948

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026