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Comparison efficacy and safety of Andrographis paniculata extract capsules and placebo in COVID-19 patients: Double blind randomized control trial

Phase 2
Completed
Conditions
COVID-19 patient with asymptomatic and mild symptomatic. Progression score between 0-3. (Green color)
COVID-19
Andrographolide
Registration Number
TCTR20210809004
Lead Sponsor
Thammasat university
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
186
Inclusion Criteria

1. Covid-19 was diagnosed within 5 day before admission in field hospital
2. Patients have asymptomatic or mild symptoms (Score is 0-3 according to WHO progression scale)

Exclusion Criteria

1. high fever (BT> 38.5 Celcius)
2. Chest X-ray was found an abnormality
3. The clinical symptoms present to pneumonia and SpO2 less than 96%
4. Started anti-viral drug before screening
5. AST and ALT more than 1.5 times of upper normal limit
6. Patient has hypersensitivity history to Andrographis
7. during on anti - coagulants drug
8. patient has serious medical condition including COPD, TB, Renal failure, heart failure, liver disease, immunodeficiancy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Symptoms everyday during on intervention VAS,severity score follow until discharge WHO progression scale
Secondary Outcome Measures
NameTimeMethod
Genomic intregrity Day 7 and Day 14 after RT-PCR show positive report Mass array
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