Comparison of thiopentone and propofol in induction of anaesthesia.

Phase 4

• Conditions: Health Condition 1: O- Medical and SurgicalHealth Condition 2: O- Medical and SurgicalHealth Condition 3: O- Medical and SurgicalHealth Condition 4: 8- Other Procedures

• Registration Number: CTRI/2023/02/049428
• Lead Sponsor: SKIMS Medical College Hospital Bemina Srinagar

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 3 April 2023

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Patients undergoing general, gynaecological or ENT surgical procedures.

Exclusion Criteria

Patients having underlying cardiological, hepatic or renal ailments.

Patients having allergy to Thiopentone or Propofol.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Induction of anesthesia <br/ ><br>vitalsTimepoint: Base line after 1 minute and 5 minutes

Secondary Outcome Measures

Name	Time	Method
ADVERSE DRUG REACTION MONITORINGTimepoint: after recovery and 4 weeks