Phenobarbital for the management of severe acute alcohol withdrawal (the PHENOMANAL trial): a pilot randomized controlled trial

Pilot and Feasibility Studies

Niall Filewod¹  Michelle Klaiman²  Alexander Caudarella²  Norman Dewhurst²  Kelly Sequeira²  Karen E. A. Burns²  Galo F. Ginocchio²  Sara Gray²  Gyan Sandhu²  Marlene Santos²  Leena Rizvi²  Danielle Buell²  Johnathan Ailon²  Stephen Hwang²  Christian J. Turner³ 

[1] Trillium Health Partners;Unity Health Toronto – St. Michael’s Hospital;University of British Columbia;

关键词: Phenobarbital;    Alcohol withdrawal;    Delirium tremens;    Treatment;   

DOI  :  10.1186/s40814-021-00963-4

来源: DOAJ

【 摘 要 】

Abstract Background Benzodiazepines are considered first-line treatment for patients experiencing severe acute alcohol withdrawal syndrome (sAAWS). Although several medications have been evaluated as potential adjuvant treatments for sAAWS, barbiturates show particular promise. Objective In the PHENOMANAL trial, we will assess the feasibility of conducting an allocation-concealed, quadruple-blinded, randomized controlled trial (RCT) comparing symptom-triggered benzodiazepine therapy with either a single dose of adjuvant intravenous (IV) phenobarbital (7.5 mg/kg of ideal body weight) or a single dose of matching IV placebo for patients with sAAWS. Methods We will recruit adult patients from the Emergency Department, Intensive Care Unit, or hospital wards with a Clinical Institute of Withdrawal – Adult revised (CIWA-Ar) score of 16 or more after receipt of at least 60 mg of diazepam or equivalent within 16 h of diagnosis of sAAWS, and an anticipated need for hospitalization. We will randomize participants (n=39) in a 2:1 manner to treatment and placebo groups, respectively. The primary objective of the PHENOMANAL pilot trial will be to demonstrate our ability to recruit the desired population over the trial period. As secondary objectives, we will evaluate clinician compliance with the treatment protocols, assess crossover rates from the placebo arm to the treatment arm, and obtain preliminary estimates of treatment effect. All trial participants will be followed for 7 days or until hospital discharge. Relevance The PHENOMANAL trial is novel in investigating a new treatment for a common and understudied condition, repurposing an existing medication for a novel indication, and addressing an important evidence gap. Through conduct of the multidisciplinary pilot trial, we aim to advance methodology in acute care research through the use of a hybrid consent model and inform the design of a large-scale trial. Trial registration ClinicalTrials.gov Registration NCT03586089 ; first registered July 13, 2018.

【 授权许可】

Unknown