Dexmedetomidine as Adjunctive Therapy for Alcohol Withdrawal

University of Colorado, Denver24 enrolled

Overview

This study is designed to evaluate dexmedetomidine as adjunctive therapy of severe alcohol withdrawal of medical ICU patients. Specifically, this study will assess whether adjunctive dexmedetomidine reduces the doses of conventional agents used for alcohol withdrawal while maintaining patient comfort and safety and will explore if dexmedetomidine exhibits a dose-dependent profile of action when it is used for this indication. In addition, this study will assess the relationships between alcohol withdrawal, therapy with dexmedetomidine, and potential serum biomarkers of alcohol withdrawal.

The objectives of this randomized, double-blind, placebo controlled, dose escalation study are a) to determine if adding dexmedetomidine to symptom-triggered, standard therapy of severe alcohol withdrawal reduces the dose requirements of conventional sedatives, analgesics, and neuroleptics; maintains patient comfort and safety; and prevents and shortens tracheal intubation; b) to explore whether dexmedetomidine acts in a dose-dependent manner to reduce the dose requirements of conventional sedatives, analgesics, and neuroleptics while maintaining patient comfort; and c) determine the association between alcohol withdrawal and potential serum biomarkers of alcohol withdrawal and assess whether these are expressed differently when dexmedetomidine is used as adjunctive therapy. Dexmedetomidine will be added to existing sedative therapies in an effort to decrease the use of these agents while maintaining patient comfort. The study will randomize twenty-four patients in a double-blind manner to receive placebo or dexmedetomidine at doses of 0.4 or 1.2 µg/kg per hour for a maximum duration of five days. All patients will be managed using an existing institution-specific, symptom-triggered alcohol withdrawal protocol.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Enrollment

Conditions

Acute Alcohol Withdrawal

Interventions

DexmedetomidineDRUG

Dexmedetomidine at 0.4 or 1.2 µg/kg per hour is administered for a maximum duration of five days

PlaceboOTHER

Normal saline for five days.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 85 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Severe alcohol withdrawal defined by a CIWA score ≥ 15 and the need for at least 16 mg of lorazepam over a four-hour period. All lorazepam doses, whether oral or intravenous, will contribute to the cumulative amount. 2. Patients receiving standard therapy for severe alcohol withdrawal according to a symptom-triggered alcohol withdrawal protocol. Lorazepam is the preferred benzodiazepine agent for patients requiring ICU admission due to alcohol withdrawal. 3. Informed consent within 36 hours of qualifying for the study. Exclusion Criteria: 1. Patients \< 18 years of age or \> 85 years of age. 2. Patients receiving benzodiazepine therapy for purposes other than alcohol withdrawal (e.g. sedation). 3. Patients with alcohol withdrawal not requiring ICU admission. 4. Patients receiving epidural administration of medication(s). 5. Comatose patients by metabolic or neurologic affectation. 6. Patients with active myocardial ischemia or second- or third-degree heart block. 7. Moribund state with planned withdrawal of life support. 8. Patients with known or suspected severe adverse reactions to dexmedetomidine (or clonidine). 9. Pregnant females or females suspected of being pregnant

Locations (1)

University of Colorado Hospital

Aurora, Colorado, United States

Outcomes

Primary Outcomes

Cumulative Lorazepam Dose Over the First Seven Days of Alcohol Withdrawal

Time frame: Seven days

Change in 12-Hour Lorazepam Requirement Pre- and Post-Treatment

Time frame: 12 hours before treatment, 12 hours after treatment on first day of starting study drug

Change in 24-Hour Lorazepam Requirement Pre- and Post-Treatment

Time frame: 24 hours before treatment, 24 hours after treatment on first day of starting study drug

Secondary Outcomes

The Degree of Alcohol Withdrawal Assessed by Clinical Institute Withdrawal Assessment (CIWA) Scores

Proportion of clinical institute withdrawal assessment (CIWA) Scores listed as severe or moderate 24 Hours after Starting Study Drug. All subjects had at least four CIWA assessments.The CIWA is a ten item scale with each item on the scale scored independently on a 0-7 or 0-4 scale, and the summation of the scores yielding an aggregate value that correlates to the severity of alcohol withdrawal. Ranges of scores are from 0 to 67. Mild alcohol withdrawal is defined with a score less than or equal to 15, moderate with scores of 16 to 20, and severe with any score greater than 20. The ten items evaluated include nausea and vomiting, tremor, sweats, anxiety, agitation, tactile disturbances, auditory disturbances, visual disturbances, headache, and orientation.

Time frame: Every 2-4 hours for 24 hours after starting study drug

The Occurrence of Adverse Events.

Occurrence of hypotension or bradycardia while on study drug

Time frame: Seven days

Plasma Epinephrine Concentrations Across Groups Over Time

Plasma epinephrine concentrations

Time frame: Four days with samples measured prior to study drug and 48 and 96 hours after starting study drug

Data from ClinicalTrials.gov

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