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NCT04183842: LACIME

Evaluation of a Fixed Combination of Herbal Extracts to Prevent Symptoms Alcohol-induced Hangovers

Completed NA Last updated 3 December 2019
What this trial tests

NA trial testing LACIME Anti-hangover in Headache in 40 participants. Completed in 7 September 2019.

Timeline
4 July 2019
Primary endpoint
26 August 2019
7 September 2019

Quick facts

Lead sponsorIncara Lab
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingquadruple
Primary purposeprevention
Enrollment40
Start date4 July 2019
Primary completion26 August 2019
Estimated completion7 September 2019
Sites1 location across Armenia

Drugs / interventions tested

Conditions studied

Sponsor

Incara Lab

Who can join

Adults 20 to 30, male only, with Headache or Nausea. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary objective of the study is to test whether the tested Product LACIME Anti-hangover is effective in preventing the signs and symptoms of alcohol-induced hangover (such as headache, impaired memory, depression, anxiety, weakness, trouble sleeping and concentrating, nausea, dizziness, sleepiness, thirsty, dry mouth, sweating, sensitivity to light and sounds, vision problems) in healthy subjects.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Headache

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04183842.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing