Reduction of pain on propofol injection after 6% Hydroxyethyl starch

Pre-Administration of 6% Hydroxyethyl Starch For Reduction of Pain on Propofol Injection: A Placebo Controlled Randomised Study - Nil

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/061670

Enrollment

100

Registered

2024-01-19

Start date

Unknown

Completion date

Unknown

Last updated

2024-01-22

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: 6% hydroxyethyl starch: with due approval from institutional ethical committee, placebo randomised study has been planned on 100 adult patients who will be undergoing General Anaesthesi

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing elective surgery under general anaesthesia ASA class 1 and 2

Exclusion criteria

Exclusion criteria: Patients undergoing emergency surgery Patients in whom hand or forearm veins are not accessible Patients with comorbidites Patient refusal

Design outcomes

Primary

Measure	Time frame
Pain during propofol injection Post operative pain recallTimepoint: Assessment of pain during propofol injection by Mc Crimick and hunter scale degree of pain during 2,5,10,20 seconds	—

Secondary

Measure	Time frame
Haemodynamic changes To compare the severity of propofol injection painTimepoint: Baseline, 5minutes, 10 minutes, 20 minutes	—

Countries

India

Contacts

Public ContactDr VEENA MATHUR

JLN medical College and hospital

veenamathur41@gmail.com9460517947

Outcome results

None listed

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