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A clinical study to evaluate the effect of Turcuron on alcohol hangover .

A Randomized Double Blind, Placebo-Controlled, Randomized, Crossover Study to Evaluate the Effectiveness, Safety and Tolerability of Turcuron (Standardized extract from Curcuma longa) in Reducing Alcohol Induced Hangover Symptoms in Adult Male Social Drinkers

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/06/019748
Enrollment
12
Registered
2019-06-18
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

None listed

Interventions

Intervention1: Turcuron: oral administration of a single dose of 400 mg Turcuron capsule for one day Control Intervention1: Placebo: oral administration of a single dose of 400 mg placebo capsule for

Sponsors

Vidya Herbs P Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Should have experienced at least one hangover previously. 2 Subjects with full comprehension and ability to understand the purpose and the nature of trial 3 Should be a non-smoker. 4 Should have no history of Alcoholic abuse i. Score of 5 Subjects with normal sleep patterns and habits. 6 Subject willing to adhere with their routine food habits, social drinking patterns and exercise regimen throughout the study 7 Must be willing and able to give informed consent and comply with the study procedures.

Exclusion criteria

Exclusion criteria: 1 History of drug dependence or excessive alcohol intake on a habitual basis of more than two units of alcoholic beverages. 2 Subjects with history of Psychiatric disorders, Seizures,Uncontrolled / serious medical illness including diabetes, liver disease, hypertension, Cardiac Disease/Neurological Problems, Gastrointestinal tract bleeding / peptic ulcer disease 3 Subjects on medications which prohibits alcohol consumption (drug interactions/contraindications). 4 Subjects who will require consumption of analgesic medications during the study. 5 Subjects who maybe allergic to any of the natural constituents of the Investigational Product. 6 History of clinically significant illness or any other medical disorder that may interfere with subject treatment, assessment or compliance with the protocol. 7 Currently participating or having participated in another clinical trial during the last 3 months prior to the beginning of this study

Design outcomes

Primary

MeasureTime frame
Changes in the alcohol hangover severity scale scoreTimepoint: Visit 2, Visit 3

Secondary

MeasureTime frame
Changes in Questionnaire based assessmentsTimepoint: Visit 2, Visit 3;Changes in Serum and Urine MarkersTimepoint: Visit 2, Visit 3

Countries

India

Contacts

Public ContactJestin V Thomas

Leads Clinical Research and Bio Services Private Limited

jestin.leadsclinbio@gmail.com9845125293

Outcome results

None listed

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