Comparison of thiopentone and propofol in induction of anaesthesia.

Comparative Study of Thiopentone and Propofol for Induction of Anaesthesia in Adults

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/02/049428

Enrollment

200

Registered

2023-02-03

Start date

Unknown

Completion date

Unknown

Last updated

2023-04-03

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 Health Condition 3: O- Medical and Surgical Health Condition 4: 8- Other Procedures

Interventions

Intervention1: Propofol: 2.5mg per kg body weight IV single dose for 2 hours for procedure Control Intervention1: Thiopentone: 4 mg per kg body weight IV single dose fir 3 hour procedure

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing general, gynaecological or ENT surgical procedures.

Exclusion criteria

Exclusion criteria: Patients having underlying cardiological, hepatic or renal ailments. Patients having allergy to Thiopentone or Propofol.

Design outcomes

Primary

Measure	Time frame
Induction of anesthesia vitalsTimepoint: Base line after 1 minute and 5 minutes	—

Secondary

Measure	Time frame
ADVERSE DRUG REACTION MONITORINGTimepoint: after recovery and 4 weeks	—

Countries

India

Contacts

Public ContactAbida Yousuf

Department of Pharmaceutical Sciences University of Kashmir

gnbader@kashmiruniversity.ac.in7006224042

Outcome results

None listed

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