To compare the effect of two methods of propofol drug delivery during induction of general anesthesia

To compare the effect of two methods of propofol delivery on pain on injection of propofol A randomized study - Nil

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/070229

Enrollment

330

Registered

2024-07-09

Start date

Unknown

Completion date

Unknown

Last updated

2026-06-01

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

Interventions

Intervention1: Method of propofol delivery on pain on injection of propofol: Group A : Patients receiving propofol 0.2mg/kg injection with lignocaine 2mg/kg pre- treatment through side port before ind

Eligibility

Inclusion criteria

Inclusion criteria: ASA I-III scheduled under GA with Propofol as the agent of intravenous induction

Exclusion criteria

Exclusion criteria: 1. Patient refusal to participate 2. Patients with known allergy to egg 3. Patients scheduled for emergency surgeries, patients with severe valvular heart disease

Design outcomes

Primary

Measure	Time frame
NRS score at 5 sec after administration of 0.2mg/kg of propofol injectionTimepoint: NRS score at 5 sec after administration of 0.2mg/kg of propofol injection	—

Secondary

Measure	Time frame
Blood pressure and heart rate at baseline and after propofol injection, any redness or inflammation at the iv cannulation siteTimepoint: At 5 seconds	—

Countries

India

Contacts

Public ContactDr Venkatesh S

Sri Ramachandra Institute of Higher Education and Research

venkymail2014@gmail.com7358697886

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026