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A randomised double-blind comparative trial investigating the level of pain experienced on induction of anaesthesia using either standard Propofol 1% or Propofol-Lipuro 1% with or without the addition of lignocaine 2% (1:10 ratio)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10285854
Enrollment
Unknown
Registered
2004-09-30
Start date
2003-08-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Surgery: Anaesthesia Surgery Anaesthesia

Interventions

1. Standard Therapy 2. New Therapy

Sponsors

Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing uncomplicated elective surgery

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
Injection pain/no pain comparison between groups—

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