Clinical Trial

The Efficacy and Safety of Reconyl in Acute Cough Treatment

Completed Phase 3
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Summary
This is a 2-arm, prospective, randomized, double-blind, parallel, controlled, non-inferiority study comparing Reconyl at a dose of 225 mg three times daily and Reconyl Placebo three times daily for a 7-day course of therapy. Reconyl is a combination of four Indonesian herbals, Vitex trifolia folium, Zingiber officinale rhizome, Abrus precatorius folium, and Phaleria macrocarpa fructus, which have been traditionally used in treating cough and common cold. A combination of these herbals is expected to relieve cough and soothe throat, provide a promising cough treatment which has no side effects.
Trial Details
NCT Number NCT07420491
Lead Sponsor Dexa Medica Group
Collaborators: PT Equilab International
Conditions Cough
Enrollment 144 participants
Start Date 2025-06-26
Primary Completion 2025-10-03 (estimated)
Study Completion 2025-10-03 (estimated)
Updated on ClinicalTrials.gov 2026-02-19