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Comparison of different doses of cisatracurium for intubation

Comparative study of three different doses of cisatracurium for tracheal intubation:A randomized clinical trial - Nill

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064130
Enrollment
45
Registered
2024-03-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Health Condition 1: - Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Administration of intravenous injection of three different doses (0.2 / 0.3 /0.4 mg/kg ) Cisatracurium: Study participants will be randomized into 3 groups. Group A recieving 0.2 mg/kg

Sponsors

Niroo
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with American Society of Anaesthesiology class 1 or class 2 2. Age 18 to 60 years of either sex. 3. Mallampatti class 1 or class 2

Exclusion criteria

Exclusion criteria: 1. Patient with allergy to study drug 2. Patients with anticipated difficult intubation 3. Pregnant and lactating patients 4. Patients receiving drugs known to interact with neuromuscular blocking agents 5. Patients with neuromuscular disorder 6. Asthmatic and psychiatric patients on medication

Design outcomes

Primary

MeasureTime frame
Onset of action of study drug Intubating scoreTimepoint: After administration of study drug untill TOF score becomes zero at baseline.

Secondary

MeasureTime frame
1. Duration of action of the study drug 2. Haemodynamic and peripheral oxygen saturation 3. Side effectTimepoint: Outcome will be continuously recorded just after administration of drug,3 minutes,5minutes then every 5 minutes untill the sign of spontaneous breathing.

Countries

India

Contacts

Public ContactDr Ashem Jack Meitei

Regional Institute of Medical Sciences

dr.saratsanasam1984@gmail.com9436027792

Outcome results

None listed

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