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Prevention of pain on injection with propofol: Comparison of lignocaine with dilution using 0.9% Sodium Chloride

Prevention of pain on injection with propofol: Comparison of lignocaine with dilution using 0.9% Sodium Chloride

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN19276105
Enrollment
Unknown
Registered
2004-09-30
Start date
2003-11-01
Completion date
Unknown
Last updated
2020-04-20

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

Conditions

Respiratory: Pain Signs and Symptoms

Interventions

Children aged 5-10 years (up to approximately 30 kg) will be randomised to either a sample or control group. A single blinded observer will then watch for signs of discomfort on induction of anaesthes

Sponsors

Department of Health
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Children aged 5-10 years (up to approximately 30 kg) with American Society of Anesthesiologists (ASA) status 1 or 2 on elective surgical lists.

Exclusion criteria

Exclusion criteria: Does not match inclusion criteria

Design outcomes

Primary

MeasureTime frame
A reduction in the incidence of pain on injection of Propofol when compared with the most commonly used and effective method in current practice (i.e. the addition of lignocaine - 2 ml 1% per 20 ml propofol).—

Secondary

MeasureTime frame
Not provided at time of registration—

Countries

United Kingdom

Outcome results

None listed

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