Baclofen to Prevent Agitation in Alcohol Addicted Patients in ICU

Last updated: January 28, 2020
Sponsor: Nantes University Hospital
Overall Status: Completed

Phase

3

Condition

Addictions

Substance Abuse

Alcohol Dependence

Treatment

N/A

Clinical Study ID

NCT02723383
RC15_0036
  • Ages 18-80
  • All Genders

Study Summary

Background: Alcohol is the leading psychoactive substance consumed in France, with about 15 million regular consumers. The National institute on Alcohol Abuse and Alcoholism (NIAAA) considers alcohol abuse to be more than 14 units of alcohol a week for men and 7 units for women. The specific complication of alcoholism is the alcohol withdrawal syndrome. Its incidence reaches up to 30% and its main complications are Delirium Tremens, restlessness, extended hospital stay, higher morbidity, psychiatric and cognitive impairment. Without appropriate treatment, Delirium Tremens can lead to death in up to 50% of patients.

Methods/Design: This prospective, randomised, controlled study versus placebo will be conducted in eighteen French intensive care units (ICU). Patients with an alcohol intake higher than the NIAAA threshold, under mechanical ventilation, will be included. The primary objective is to determine whether Baclofen is more efficient than placebo in preventing restlessness-related side effects in ICU. Secondary outcomes include mechanical ventilation duration, length of ICU stay, cumulative doses of sedatives and painkillers received within 28 days of ICU admission. Restlessness-related side effects are defined as unplanned extubation, Medical disposal removal, falling out of bed, ICU runaway, immobilisation device removal, self-aggression or towards medical staff. Daily doses of Baclofen/placebo will be guided by creatinine clearance assessment once a day.

Discussion: Restlessness in alcoholic patients is a life-threatening issue in ICUs. BACLOREA is a randomised study assessing the capacity of Baclofen to prevent agitation in mechanically-ventilated patients. Enrolment of 314 patients will begin in June 2016 and is expected to end in December 2019.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Adults from 18 to 80 years old with an estimated alcohol intake of:

  • 14 units of alcohol per week during the month before hospitalisation for men aged 18 to 64

  • 7 units of alcohol per week during the month before hospitalisation for women ormen older than 65. AND Intubated, ventilated with an expected duration of mechanical ventilation> 24 hours atleast

Exclusion

Exclusion Criteria:

  • Hospitalization > 7 days

  • Baclofen administration before ICU admission (personal treatment or singleadministration)

  • Pregnancy

  • Porphyria

  • Burned on ICU admission

  • Personal treatment including Gamma-hydroxybutyric acid (Alcover/Xyrem)

  • Recent stroke or subarachnoid haemorrhage or head trauma with radiological evidence

  • Recent or old paraplegia or tetraplegia

  • Cardiac arrest with resuscitation manoeuvres before or after ICU admission

  • Contraindication to Enteral drug administration for longer than 24 hours

  • Lack of social protection

  • Hypersensitivity to Baclofen

  • Coeliac disease

  • Refractory epilepsy

  • Dementia, schizophrenia, Bipolar disorder or severe depression.

  • Parkinson's disease

  • Health care limitation owing to pejorative prognosis

  • Tracheotomy on ICU admission

  • Patients under guardianship or trusteeship

  • Patients already enrolled in interventional study

Study Design

Total Participants: 314
Study Start date:
June 27, 2016
Estimated Completion Date:
August 14, 2019

Connect with a study center

  • CHU ANGERS - réanimation chirurgicale

    Angers,
    France

    Site Not Available

  • CHU de Brest Réanimation Chirurgicale

    Brest,
    France

    Site Not Available

  • CHU de Brest Réanimation Médicale

    Brest,
    France

    Site Not Available

  • CHU de Caen Réanimation Médicale

    Caen,
    France

    Site Not Available

  • CHD La Roche Sur YON

    La Roche Sur Yon,
    France

    Site Not Available

  • CH Le Mans

    Le Mans,
    France

    Site Not Available

  • Centre Hospitalier de Bretagne Sud Réanimation Polyvalente Lorient

    Lorient,
    France

    Site Not Available

  • CHU MONTPELLIER - Lapeyronie

    Montpellier,
    France

    Site Not Available

  • Chu Montpellier

    Montpellier,
    France

    Site Not Available

  • CHU NANTES - réanimation chirurgicale

    Nantes,
    France

    Site Not Available

  • CHU NANTES -réanimation médicale

    Nantes,
    France

    Site Not Available

  • Hopital Saint Antoine

    Paris,
    France

    Site Not Available

  • Chu Poitiers

    Poitiers,
    France

    Site Not Available

  • Ch Cornouaille

    Quimper,
    France

    Site Not Available

  • Chu Rennes

    Rennes,
    France

    Site Not Available

  • CHR Saint Nazaire

    Saint Nazaire,
    France

    Site Not Available

  • CHRU Tours Bretonneau

    Tours,
    France

    Site Not Available

  • Chu Tours

    Tours,
    France

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.