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CompletedNCT04542876Updated Sep 9, 2020

Efficacy and Safety of Guduchi Ghan Vati in the Management of Asymptomatic COVID-19 Infection

An interventional study of Guduchi Ghan Vati in Covid19, sponsored by Aarogyam UK. Completed at 1 site in India. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-09-09.

Sponsored by Aarogyam UK · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 4 months after the study started (first participant enrolled May 2020, registered Sep 2020).
Phase
Not applicable
Study type
Interventional
Enrollment
46
Allocation
Not applicable
Ages
18 Years and older
Sex
All
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Study summary

The emergence of asymptomatic patients poses a significant challenge to the prevention and treatment of the epidemic.There have not been any treatment options that reduce the viral load or preventive options that reduce the risk of developing severe conditions.Therefore, present feasibility study of the safety and efficacy of Guduchi Ghan Vati was conducted in asymptomatic patients with COVID-19

02

Conditions studied

  • Covid19

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03

In context

COVID-19

7,641 studies on the registry are indexed under COVID-19; 487 are open to participants now.

This study's enrollment of 46 is below the median of 100 across 4,100 interventional studies indexed under COVID-19.

Browse COVID-19 studies →

Lead sponsor

Aarogyam UK is the lead sponsor of 19 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • All hospitalised cases above 18 years of age,
  • Diagnosed with Covid-19
  • Asymptomatic at the time of admission
  • Agree to give consent

Exclusion criteria

Exclusion Criteria:

  • Symptoms relating to Covid-19
  • Severe vomiting
  • Respiratory failure or requiring mechanical ventilation
  • Patients having alanine transaminase (ALT) or aspartate transaminase (AST) > 5 times the upper range of normal limits
  • Patients with Covid-19 in critical condition or ARDS or NIAD 8 -point ordinal score-2
  • Patients with uncontrolled diabetes mellitus
  • Malignant,
  • Chronic renal failure or
  • On immunosuppressive medication
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
46 participants (actual)

Study arms

  • Experimental
    Ayurveda

    Guduchi Ghana is a unique Ayuvedic classical preparation prepared from aqueous extracts of Tinospora cordifolia stem.

    Drug: Guduchi Ghan Vati

Interventions

  • DrugGuduchi Ghan Vati

    Guduchi Ghan Vati was orally administered 2 tablets (1000 mg) twice daily for 2 weeks.

    Also known as: Giloya, Amrita, Tinosporia Cordifolus, Guduchi

06

What researchers measure

Primary outcomes

  1. Virologic clearance

    Virologic clearance indicates the duration from the first Covid-19 positive result to the first Covid-19 negative result

    Time frame: 14 days

Secondary outcomes

  1. Hospital Stay

    Total duration of stay in hospital for complete recovery

    Time frame: 14 days

  2. Clinically relevant adverse effects

    Clinically relevant adverse effects of Guduchi Ghan Vati were reported using Adverse Drug Reaction reporting form

    Time frame: 14 days

  3. Laboratory tests

    Routine blood tests were performed to assess complete blood counts, blood biochemistry parameters {Aspartate aminotransferase (AST), Alanine aminotransferase (ALT), Urea, C-reactive protein (CRP), as well as Albumin} and immunoglobulines.

    Time frame: change from baseline to 14 days

07

Study locations

1 site
  • Dr. Sarvepalli Radhakrishnan Rajasthan Ayurved University
    Jodhpur, Rajasthan, India
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 9, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04542876
Lead sponsor
Aarogyam UK
Collaborators
Dr. Sarvepalli Radhakrishnan Rajasthan Ayurved University
Responsible party
Sponsor
First posted
Sep 9, 2020
Start date
May 1, 2020
Primary completion
Jul 31, 2020
Completion
Aug 18, 2020
Last update
Sep 9, 2020

Study contacts

Abhimanyu Kumar
principal investigator · Dr. Sarvepalli Radhakrishnan Rajasthan Ayurved University
Neha Sharma
study director · Aarogyam UK

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2020. You cannot join it, but the record below documents what was studied.

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