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NCT04395976 Clinical Trial

Ayurveda as Prophylaxis for Suspected COVID-19 Patients

Covid-19 Clinical Trial

Official title:
Effect of Ayurveda as Prophylaxis for Suspected Covid-19 Patients: Randomised Controlled Trial

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT04395976
Other study ID # BAMC01
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date May 10, 2020
Est. completion date September 1, 2020

Study information
Verified date February 2021
Source British Ayurvedic Medical Council
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Despite worldwide efforts to contain, manage and treat Covid-19, the pandemic is continuing to spread. This calls for an urgent clinically-proven prophylaxis and therapeutic strategy. Recent developments on the use of traditional medicines in Covid-19 management has drawn enough attention to start several research studies. Based on the Indian Traditional Medicine, Ayurveda's community initiatives, preliminary studies, and our experiential knowledge on Covid-19 settings, we propose present study to prevent the development of COVID-19 symptoms in people who live or have come contact with an individual diagnosed with COVID-19.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date September 1, 2020
Est. primary completion date June 10, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Person who has come into contact with confirmed COVID-19, - Willing to take study drug as directed Exclusion Criteria: - Confirmed current COVID-19 - Inability to take medications orally - Inability to provide written consent

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Ayurveda
The Ayurveda intervention is multimodal and following the principles of Ayurveda as a whole medical system, each participants will be treated with individualised care. From the range of proven Ayurvedic Herbs, combination will be decided based on individual participants, his symptoms and his personality.

Locations
Country Name City State
United Kingdom British Ayurvedic Medical Council London

Sponsors (3)
Lead Sponsor Collaborator
British Ayurvedic Medical Council All Party Parliamentary Group - Indian Traditional Sciences, University of Warwick

Country where clinical trial is conducted

United Kingdom, 

Outcome
Type Measure Description Time frame Safety issue
Primary Clinical confirmation of Covid-19 Number of participants with symptomatic, lab-confirmed COVID-19 From date of enrolment to 14 days
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