The effect of emulsion formulation on Propofol injection pain

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN35049639

Enrollment

200

Registered

2004-09-30

Start date

2003-05-01

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

Interventions

Patients were allocated randomly into two groups to receive either Propofol-Lipuro without added lidocaine or Diprivan mixed with lidocaine 10 mg. 5 ml of the study solution was injected at a constant

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients scheduled for surgery requiring general anaesthesia in whom Propofol is an appropriate anaesthetic induction agent

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

Measure	Time frame
Injection pain experienced by patients during induction of general anaesthesia	—

Secondary

Measure	Time frame
Not provided at time of registration	—

Countries

United Kingdom

Outcome results

None listed

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