Chronic alcoholism increases the induction dose requirements of propofol in patients anesthetized with propofol and remifentanil by target-controlled infusion

Status

Active, not recruiting

Phases

Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR-OCC-11001224

Enrollment

Unknown

Registered

2011-03-03

Start date

2010-02-01

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

alcohol abuse

Interventions

A:chronic alcoholism, pain stimulus

B:non-alcoholism, pain stimulus

Eligibility

Sex/Gender

Male

Age

25 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Sign the informed content forms; 2. Daily alcohol intake more than 75g (study group)

Exclusion criteria

Exclusion criteria: liver dysfunction

Design outcomes

Primary

Measure	Time frame
concentration for 50% of maximum effect;	—

Countries

China

Contacts

Public ContactChao LIANG

superwm226@yahoo.cn+86 15921679955

Outcome results

None listed

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