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Dosage determination and efficacy of propofol and atracurium for rapid sequence induction of anesthesia: A randomized double-blind prospective study.

Determination of dosage and effectiveness of propofol and atracurium for rapid sequence induction of anesthesia: A Prospective double-blind controlled study.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20170912003
Enrollment
Unknown
Registered
2017-09-12
Start date
2017-09-13
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Emergency surgery required rapid sequence induction of anesthesia Rapid sequence induction&#44

Interventions

Standard dose 0.6 mg/kg for intubation,Use atracurium 0.75 mg/kg for intubation,Use atracurium 1 mg/kg for intubation
Active Comparator Drug,Active Comparator Drug,Active Comparator Drug
Controlled group,Atracurium 0.75,Atracurium 1

Sponsors

The Royal College of Anesthesiologists of Thailand (RCAT)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective surgery, aged 20-65 years, and require general anesthesia 2. ASA physical status I-II

Exclusion criteria

Exclusion criteria: 1. Patients required emergency surgery 2. Unstable vital signs 3. History of difficult intubation or anticipated difficult intubation 4. Patients with history of neuromuscular disease 5. On anticonvulsant medication for more than 1 month 6. History of asthma or use bronchodilators 7. History of allergy to medications used in the study 8. Obesity, BMI >30

Design outcomes

Primary

MeasureTime frame
Intubating condition 1 minute after drug administration Likert scale for vocal cord and diaphragm movement during intubation

Secondary

MeasureTime frame
Muscle blockade of atracurium TOF=0 Train-of-four (TOF),Muscle power recovery time TOF=2 Train-of-four (TOF),Hemodynamic 10 minutes after study drug administration BP, HR,adverse effect from study drug 10 minutes after study drug admistration rash, bronchospasm (high airway pressure)

Contacts

Public ContactPornpan Chalermkitpanit

Chulalongkorn University

pornpan.c@chula.ac.th+66894554847

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026