Propofol and remifentanil requirements after acute ethanol intake in clinical settings

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN73421343

Enrollment

Registered

2005-07-08

Start date

2004-02-02

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

Interaction of acute ethanol intravenous intake with propofol (general anesthetic) and remifentanil (opioid) Surgery Anaesthesia

Interventions

Comparison of two groups (with different ethanol doses) versus control (no ethanol), regarding propofol and remifentanil requirements

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Female surgical patients on general anesthesia

Exclusion criteria

Exclusion criteria: Alcoholic patients, patients in abstinence

Design outcomes

Primary

Measure	Time frame
Reduction of propofol and remifentanil requirements	—

Secondary

Measure	Time frame
Degree of reduction, side-effects	—

Countries

Greece

Outcome results

None listed

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