Alcohol Cessation Intervention in an Acute Surgical Setting

Status Completed

Clinical Trial Summary

Hazardous alcohol intake is an independent risk factor for postoperative complications after major and minor operations, elective and emergency procedures for men and women.

The aim of this study is to evaluate the effect of a 6-week Gold Standard Programme for alcohol cessation intervention in the perioperative period compared to the daily routine guidelines for patients with hazardous alcohol intake undergoing ankle fracture surgery.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00986791
Study type	Interventional
Source	Bispebjerg Hospital
Contact
Status	Completed
Phase	N/A
Start date	May 2010
Completion date	March 2018

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