This study aims to evaluate the efficacy and safety of Herbamuno+, a combination ofseveral herbal ingredients, as an adjunct therapy for moderate COVID-19 patients at WismaAtlet. The study involves 66 patients who were divided into two groups: one receivingHerbamuno+ and the other a placebo, both for 14 days. Researchers monitored clinicalimprovements, 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 tostandard COVID-19 treatment.
Not Provided
Other: Placebo
The placebo contains the non-active carrier of herbal combination that has no
pharmacological activity.
Dietary Supplement: herbal compound
The 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.
Inclusion Criteria:
- The RCT included patients who met the following criteria: >18 years old,
had recently tested positive for COVID-19 through RT-PCR within the past five days,
and were categorized as moderate cases. The main clinical symptoms required for
inclusion were acute fever (greater than 38 °C) and cough, or more than three of the
following acute symptoms or signs: fever, cough, fatigue, headache, muscle pain,
sore throat, nasal congestion, runny nose, shortness of breath, anorexia, nausea,
vomiting, diarrhea, anosmia, or ageusia. The moderate case criteria are based on WHO
criteria including the radiology imaging that indicating pneumonia (new infiltrates
to consolidation) and clinical signs of pneumonia (fever, cough, shortness of
breath, and respiratory frequency between 20 to 30 times per minute).
Exclusion Criteria:
- Patients were excluded if they had any of the following conditions: an oxygen
saturation of less than 93%, participating in other clinical trials, pregnant or
lactating, receiving other immunomodulatory drugs, had a history of allergies to the
test product, or the history of tuberculosis, HIV/AIDS, psychosis, or autoimmune
disorders. Subjects may also be dropped from the clinical trial if they withdraw,
fail to comply with the protocol (including using less than 80% of the test
product), disappear, or no longer meet the inclusion criteria. Adverse events,
worsening conditions, or new diagnoses during the trial also warrant exclusion.
The National Emergency Hospital for COVID-19, Wisma Atlet
Jakarta 1642911, DKI Jakarta, Indonesia
Not Provided