Alkontrol-herbal Effects on Alcohol Drinking

Alcohol Use Disorder Clinical Trial

— Alkontrol  

Official title:

Alkontrol-herbal (Isoflavone) Effects on Alcohol Drinking in an Outpatient Setting

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03099590
• Other study ID #: 2017P000109
• Status: Completed
• Phase: Phase 2
• Start date: January 1, 2018
• Est. completion date: July 1, 2020

Study information

• Verified date: July 2020
• Source: Mclean Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Participants will enroll in a 14-week study (2 weeks of baseline, 8 weeks of treatment, and 4 weeks of follow-up) investigating the impact that Alkontrol-herbal (Isoflavone; Kudzu) has on alcohol intake in a population seeking treatment for an alcohol use disorder.

Description:

Over the past 15 years, the Behavioral Psychopharmacology Research Lab at McLean Hospital has extensively studied kudzu extract and demonstrated its safety and efficacy in healthy control subjects as well as in heavy binge drinkers. The relative success of our recent outpatient trial of kudzu extract demonstrated a modest decrease in drinking, reduction in the number of heavy drinking days, and significant increase in the number of days abstinent. This suggests that Alkontrol-herbal, kudzu extract, may be a useful adjunct in treating alcohol use disorders.

Participants will enroll in a 14-week study (2 weeks of baseline, 8 weeks of treatment, and 4 weeks of follow-up) investigating the impact that Alkontrol-herbal has on alcohol intake in a population (age 21-60 years) seeking treatment for an alcohol use disorder. Participants will take 500 mg of a crude kudzu extract (NPI-031, Alkontrol-herbal; Natural Pharmacia International, Burlington, MA) t.i.d.; matched sugar beet placebo capsules will serve as placebo. Subjects will come to the lab three times a week to provide urine samples that can be tested for medication compliance through a biochemical marker, acetazolamide, included in the medication capsules. Participants will record their alcohol intake through daily diaries and a wrist actigraphy device, which will also monitor their sleep/wake activity.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 28
• Est. completion date: July 1, 2020
• Est. primary completion date: March 1, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years to 60 Years

Eligibility

Inclusion Criteria:

• Subject can understand and comply with the protocol

• Good physical and mental health (normal physical exam, ECG, blood and urine chemistries, including absence of history or laboratory evidence of diabetes)

• Body Mass Index between 18-30, inclusive

• Age 21-60 years (age will be verified by driver's license or other valid form of identification)

• Meet criteria for current Moderate or Severe (4+ symptoms) Alcohol Use Disorder per the DSM-5; If attending a self-help treatment group (e.g., AA) at time of the screening visit, subject must agree to continue attending these groups for the duration of the study

• Seeking treatment for an Alcohol Use Disorder

• Drink 20-35 (or more) drink per week

• Report drinking on 80% of days in the past 90 days

• Have a stable living situation with current postal address

Exclusion Criteria:

• Subject meets DSM-5 criteria for major depression and/or bipolar disorder, and is not medically, pharmacologically, or clinically stable. Subjects who currently meet criteria for minor depression or bipolar disorder and have been clinically stable (including medications) for the past 2 months may participate in the study, at the investigator's discretion

• Concurrent diagnosis of any other Axis I disorder, including any substance use disorder besides alcohol use disorder Maintained on an antipsychotic or anti-seizure medication; Current prescription for benzodiazepines

• Presence of neurological, infectious, or neoplastic disease or a chronic medical disorder

• Tobacco use greater than 10 cigarettes per day

• Currently abstaining from consuming alcoholic beverages longer than 10 days

• History of major head trauma resulting in cognitive impairment or history of seizure disorder

• Heavy caffeine use (greater than 500 mg on a regular, daily basis)

• Subject has active hepatitis and/or aspartate aminotransferase (AST), alanine aminotransferase (ALT) > 3x the upper limit of normal

• For female volunteers, a positive pregnancy test (female subjects must agree to an approved method of contraception for the duration of the study)

Related Conditions & MeSH terms

• Alcohol Abstinence
• Alcohol Drinking
• Alcohol Use Disorder
• Alcoholism

Intervention

Dietary Supplement:
• kudzu extract, puerarin
Capsules containing 500 mg of a crude kudzu extract (NPI-031, Alkontrol-herbal; Natural Pharmacia International, Burlington, MA) will be used, containing 19% puerarin, 4% daidzin and 2% daidzein, so each capsule contains a total of 25% active isoflavones or 125 mg.
• Placebo control
Matched sugar beet placebo capsules will serve as placebo.

Locations

Country	Name	City	State
United States	McLean Hospital	Belmont	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Mclean Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	percent days abstinent	percent days abstinent from alcohol	change from baseline to post 8 weeks of treatment
Primary	drinks/day	number of alcoholic drinks/day reported	change from baseline to post 8 weeks of treatment
Primary	number (or percent) of heavy drinking days	number (or percent) of heavy drinking days	change from baseline to post 8 weeks of treatment
Primary	percent days abstinent	percent days abstinent from alcohol	change from baseline to 4 weeks follow-up post-treatment
Primary	drinks/day	number of alcoholic drinks/day reported	change from baseline to 4 weeks follow-up post-treatment
Primary	number (or percent) of heavy drinking days	number (or percent) of heavy drinking days	change from baseline to 4 weeks follow-up post-treatment