studying the blood pressure and pulse rate changes with relation to different timing of propofol drug administration

A Study to compare the haemodynamic changes with and without Priming Principle with Propofol induction - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/07/090651

Enrollment

Registered

2025-07-10

Start date

Unknown

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

Health Condition 1: K353- Acute appendicitis with localizedperitonitis

Interventions

Intervention1: PRIMING: PRIMING WITH INJ.PROPOFOL 25% OF 2mg/kg before induction of general anaesthesia. 3min Control Intervention1: NORMAL SALINE IS THE COMPARATOR AGENT.: 3CC

Eligibility

Inclusion criteria

Inclusion criteria: Asa Grade I and grade II Patients undergoing elective surgeries under general anaesthesia.

Exclusion criteria

Exclusion criteria: Known allergy to propofol History of opioid abuse Pregnant and lactating women

Design outcomes

Primary

Measure	Time frame
Reduction in induction dose of propofol and hemodynamic stabilityTimepoint: Reduction in induction dose of propofol and hemodynamic stability Immediately after induction and At 3min,5min ,10min after induction	—

Secondary

Measure	Time frame
Haemodynamic stabilityTimepoint: Immediately after induction, at 3min,5min,10min after induction	—

Countries

India

Contacts

Public ContactDRLATA A SHAH

Mahadevappa Rampure Medical college

latads@yahoo.co.in9731046446

Outcome results

None listed

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