Caron Ketone AUD withdrawal study

Recruiting
99 years and younger
All
Phase N/A
1 Location

Brief description of study

To examine the effects of ketone supplement, Kenetik (KS) three times daily (TID), verse placebo, on the need for benzodiazepines and CIWA scores, while undergoing in-patient acute withdrawal management.To test the effects of Ketone Supplementation (KS) Kenetik in reducing alcohol withdrawal signs and symptoms and the need for medications to control them (benzodiazepines and comfort medications) in AUD inpatients during alcohol detoxification The primary outcome variable the daily amount of Benzodiazepine intake during the first 5 days of alcohol withdrawal management. We expect that subjects treated with KS will require less benzodiazepine medication than the placebo group. The secondary outcome variable is the total daily maximum CIWA-Ar score during the first week of alcohol withdrawal management. We expect that subjects treated with KS will have lower daily maximum CIWA-AR scores during the 5 days of alcohol withdrawal management.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Medical Research
  • Age: - 99 Years
  • Gender: All

TBD

Updated on 01 Aug 2024. Study ID: 854682

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