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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
314
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.
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.
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
...and 8 more locations
Occurrence (yes or no) of agitation-related adverse events
Occurrence (yes or no) of agitation-related adverse events during treatment/placebo administration with at least one sign out of the following: * Unplanned extubation * Medical disposal removal * Falling out of bed * ICU runaway * Immobilization device removal * Self-aggression or aggression towards medical staff.
Time frame: at the end of treatment (22 days max)
Adverse event (yes or no) related to agitation
Time frame: within 28 days of ICU admission
Extubation failure defined as reintubation
Time frame: within the next 48 hours after extubation
Tracheotomy for failure of mechanical ventilation weaning during hospitalization
Time frame: an average of 28 days
Infections acquired in the ICU: Urinary infection, pneumonia, catheter infection or bacteraemia during hospitalization
Time frame: an average of 28 days
Total doses of sedatives and painkillers received in the ICU
Time frame: within 28 days of ICU admission
Riker Sedation -Agitation Scale (SAS) in the ICU
Time frame: within 28 days of ICU admission
Daily CIWA-Ar alcohol withdrawal score
Time frame: during the week following extubation
Duration of mechanical ventilation during hospitalization
Time frame: an average of 28 days
Ventilation free days (VFD)
Time frame: at day 28
Length of ICU stay
Time frame: within 90 days
Length of total hospitalisation
Time frame: within 90 days
Death in ICU
Time frame: at days 28 and 90
Death during hospital stay during hospitalization
Time frame: within 90 days
Number of adverse event (s) per patient occurring in ICU from Day 1 to Day 28
Time frame: until Day 28
Agitation requiring rapid intravenous or intramuscular administration of an hypnotic or neuroleptic (bolus)
Time frame: until Day 28
Reintubation due to restlessness or withdrawal syndrome
Time frame: until Day 28
Agitation and mortality in ICU at Day 28
Time frame: at Day 28
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.