Clinical Research Directory
Browse clinical research sites, groups, and studies.
Baclofen to Prevent Agitation in Alcohol Addicted Patients in ICU
Sponsor: Nantes University Hospital
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.
Official title: Baclofen to Prevent Agitation in Alcohol Addicted Patients in ICU: Study Protocol for a Randomised Controlled Against Placebo Trial
Key Details
Gender
All
Age Range
18 Years - 80 Years
Study Type
INTERVENTIONAL
Enrollment
314
Start Date
2016-06-27
Completion Date
2019-08-14
Last Updated
2026-09-14
Healthy Volunteers
No
Conditions
Interventions
BACLOFEN
Daily doses will be adapted to daily MDRD creatinine clearance from 150 to 50mg. On the day of randomisation, the patient will receive the full daily dose in a one-shot administration. Then daily doses will be divided into 3 intakes on the following days. During the mechanical ventilation period, the treatment will be administered via the nasogastric feeding tube. After extubation, the treatment will be administered either via the nasogastric tube or the oral route.
PLACEBO
Daily doses will be adapted to daily MDRD creatinine clearance from 150 to 50mg. On the day of randomisation, the patient will receive the full daily dose in a one-shot administration. Then daily doses will be divided into 3 intakes on the following days. During the mechanical ventilation period, the placebo will be administered via the nasogastric feeding tube. After extubation, the placebo will be administered either via the nasogastric tube or the oral route.
Locations (18)
CHU ANGERS - réanimation chirurgicale
Angers, France
CHU de Brest Réanimation Chirurgicale
Brest, France
CHU de Brest Réanimation Médicale
Brest, France
CHU de Caen Réanimation Médicale
Caen, France
CHD La Roche Sur YON
La Roche-sur-Yon, France
CH Le Mans
Le Mans, France
Centre Hospitalier de Bretagne Sud Réanimation Polyvalente Lorient
Lorient, France
CHU MONTPELLIER - Lapeyronie
Montpellier, France
Chu Montpellier
Montpellier, France
CHU NANTES - réanimation chirurgicale
Nantes, France
CHU NANTES -réanimation médicale
Nantes, France
Hopital Saint Antoine
Paris, France
Chu Poitiers
Poitiers, France
Ch Cornouaille
Quimper, France
Chu Rennes
Rennes, France
CHR Saint Nazaire
Saint-Nazaire, France
CHRU Tours Bretonneau
Tours, France
Chu Tours
Tours, France