Clinical Trials Directory

Trials / Completed

CompletedNCT06636760

Efficacy and Immunomodulator Impact of Herbal Combination on COVID-19 Patients Recovery

Efficacy and Safety of Herbal Combination As Adjuvant Therapy for Mild and Moderate COVID-19 Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
66 (actual)
Sponsor
Indonesia University · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

This study aims to evaluate the efficacy and safety of Herbamuno+, a combination of several herbal ingredients, as an adjunct therapy for moderate COVID-19 patients at Wisma Atlet. The study involves 66 patients who were divided into two groups: one receiving Herbamuno+ and the other a placebo, both for 14 days. Researchers monitored clinical improvements, chest X-rays, and blood tests to assess inflammation and immune response. The goal is to determine whether Herbamuno+ can be safely and effectively added to standard COVID-19 treatment.

Conditions

Interventions

TypeNameDescription
OTHERPlaceboThe placebo contains the non-active carrier of herbal combination that has no pharmacological activity.
DIETARY_SUPPLEMENTherbal compoundThe herbal combination is made up of various medicinal plants and possesses immunomodulator properties. It comprises Phyllanthus niruri, Andrographis paniculata, and Glycyrrhiza glabra, along with Anacardium occidentale leaf and Zingiber officinale rhizome, all recognized for their immunomodulatory properties.

Timeline

Start date
2021-08-27
Primary completion
2022-03-28
Completion
2022-03-28
First posted
2024-10-15
Last updated
2024-10-15

Locations

1 site across 1 country: Indonesia

Source: ClinicalTrials.gov record NCT06636760. Inclusion in this directory is not an endorsement.