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Administering anaesthesia using two different intravenous agents for et insertion in trachea

Comparison of Propofol Auto-coinduction and standard Propofol induction technique for laryngoscopy and intubation.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046455
Enrollment
80
Registered
2022-10-13
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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 Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Propofol Autocoinduction: Autocoinduction technique is used to reduce dose and side effect of propofol Control Intervention1: Standard Propofol induction: Standard propofol induction is

Sponsors

Government of Gujarat
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Elective or emergency surgery, Given written & informed consent, modified mallampatti classification I, II, & III , BMI < 25, hypertensives,

Exclusion criteria

Exclusion criteria: Refusing consent , already on opioid analgesic , phenothiazine , tranquilliser, sedatives, hypnotic, and other CNS depressant, BMI > 30 , Ristricted neck movement, History of gastro& esophageal reflux, hiatus hernia , pregnancy, patient having pharyngeal pathology

Design outcomes

Primary

MeasureTime frame
Propofol Autocoinduction is beneficial to reduce dose and side effectTimepoint: Starting From Premedication to 30 min after induction—

Secondary

MeasureTime frame
Propofol Autocoinduction also reduce pain of propofol and other side effectTimepoint: 30 minutes after Autocoinduction—

Countries

India

Contacts

Public ContactDr Tarlika P Doctor

B J medical college , Ahmedabad

tpdoctor@hotmail.com9825353377

Outcome results

None listed

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