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Intravenous colloid infusions for prevention of pain on propofol injection

Effect of 6% hydroxyethyl starch (130/0.4) for prevention of pain on propofol injection: randomized control trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/05/025000
Enrollment
130
Registered
2020-05-04
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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 (130/0.4): 100 ml (bolus), once, i.v, before administration of anesthesia Control Intervention1: Normal Saline 0.9%: 100 ml (bolus), once, i.v, before administra

Sponsors

Dr Satyajeet Misra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I and II patients undergoing elective surgery under general anaesthesia

Exclusion criteria

Exclusion criteria: Hypertensives; diabetics; known LV dysfunction; known allergy to Propofol or hydroxyethyl starch

Design outcomes

Primary

MeasureTime frame
Pain on propofol injectionTimepoint: During administration of propofol while giving anesthesia—

Secondary

MeasureTime frame
Patient satisfactionTimepoint: 2 hours after recovery from anesthesia—

Countries

India

Contacts

Public ContactDr Satyajeet Misra

All India Institute of Medical Sciences (AIIMS), Bhubaneswar

misrasatyajeet@gmail.com

Outcome results

None listed

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