Study on safety and efficacy of an Ayurvedic formulation on Alcoholism

Analytical and Experimental Study of Sumukti An Indigenous Formulation and its Controlled Clinical Evaluation on Alcohol Dependency

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2017/03/008024

Enrollment

Registered

2017-03-07

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Alcohol dependency

Interventions

Intervention1: Sumukti Syrup: Ayurvedic compound formulation Sumukti 15ml orally thrice a day half an hour before food for 30 days Control Intervention1: Sreekandasava: Ayurvedic compound formulation

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects with signs & symptoms of Madatyaya [symptoms of alcohol dependence as per ICD - 10] 2. Age limit- 18- 50 years 3. Subjects of both sex

Exclusion criteria

Exclusion criteria: • Subjects suffering from other systemic diseases like diabetic mellitus and hypertension • Subjects suffering from chronic liver diseases like liver cirrhosis • Subjects suffering from organic brain diseases

Design outcomes

Primary

Measure	Time frame
Subjective and objective symptoms of Alcohol dependencyTimepoint: Assessment of clinical study will be done on day 0(Baseline), after 15 days and end of 30 days	—

Secondary

Measure	Time frame
Lipid profileTimepoint: 9 months	—

Countries

India

Contacts

Public ContactDr Prasanna N Rao

DM College of Ayurveda and Hospital

drsuhasshetty@gmail.com9449603234

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026