Safety and Efficacy Reconyl for Cough With/Without Sore Throat

Dexa Medica Group60 enrolled

Overview

This study is a prospective, randomized, double-blind and placebo-controlled study to find out if reconyl may relieve the acute cough with/without sore throat.

Reconyl is a mixed extract from 4 Indonesian herbs, Vitex trifolia (Legundi), Zingiber officinale var. Amarum (Jahe Gajah), Abrus precatorius (Saga), and Phaleria macrocarpa (Mahkota Dewa), which have been known traditionally to relieve cough, respiratory congestion, and sore throat. There will be two parallel groups of 30 subjects per group (a total of 60 subjects) planned to be enrolled in this study. The investigational product: tablets @ 225 mg of Reconyl. Dose administration: One tablet of Reconyl or Placebo, given 3 times daily, for 3 days. Eligible subjects will be instructed to perform a daily self-assessment on the cough symptoms over the 3 days of treatment, in the Subject Diary. Subject shall return to the study clinic 3 days ± 24 hours after the first dose, for completion of the subject's participation in the study.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Enrollment

Conditions

Cough

Interventions

ReconylDRUG

1 tablet of Reconyl, 3 times daily

Placebo tablet of ReconylDRUG

1 tablet of placebo Reconyl, 3 times daily

Eligibility

Sex: ALLMin age: 18 YearsMax age: 60 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Healthy men or women aged 18 to 60 years with cough with/without sore throat with a maximum onset of 3 days. 2. Signing the informed consent. Exclusion Criteria: 1. Body temperature of \> 37.3˚C and/or refuse to follow health protocol for COVID-19 2. Known hypersensitivity to herbal drugs 3. Pregnant or lactating women 4. Have received any anti-inflammatory or cough-alleviating drugs within the past 24 hours 5. Presence of vomiting or diarrhea within the past 24 hours and still ongoing at the start of study 6. Severe illness, e.g. severe hypertension, any other chronic infections or diseases that may induce cough, such as: pulmonary tuberculosis, gastrointestinal reflux diseases (GERD)

Locations (2)

Imeri Fkui

Jakarta Pusat, DKI Jakarta, Indonesia

Klinik Satelit Makara UI Depok

Depok, West Java, Indonesia

Outcomes

Primary Outcomes

Cough score

Scoring will be performed and recorded daily in the Subject Diary at time 0, every night time and before the morning dose. At the End of Study (last visit) will be assessed by the subject and recorded by the Investigator. Cough score: • Day time: 0 = No cough; 1= Transient cough occasionally during the daytime; 2 = Frequent cough mildly affecting daily life; 3 = Frequent cough severely affecting daily life. • Night time: 0 = No cough; 1= Transient cough before sleep or occasional cough during the night; 2 = Cough mildly affecting night sleep; 3 = Cough severely affecting night sleep.

Time frame: Day 0, Day 1, Day 2, Day 3

Visual Analogue Scale (VAS)

Visual Analogue Scale (VAS) for sore throat (0 - 100), with 0 indicates asymptomatic and 100 refers to the most serious or severe symptom. VAS will be assessed and recorded daily in Subject Diary at time 0, every night time and before the morning dose. At the End of Study (last visit) will be assessed by the subject and recorded by the Investigator.

Time frame: Day 0, Day 1, Day 2, Day 3

Adverse events

Any adverse events (AE) and serious adverse events (SAE) will be observed throughout the study conduct.

Time frame: Day 0, Day 1, Day 2, Day 3

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.