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An interventional study to access the effect of Homoeopathic medicine in positive cases of COVID-19.

A prospective double blind randomised controlled trial of Eupatorium perfoliatum 30 C in asymptomatic and mild symptomatic cases of COVID-19.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/07/026757
Enrollment
200
Registered
2020-07-23
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere

Interventions

Intervention1: Eupatorium perfoliatum 30 C: Eupatorium perfoliatum 30 C twice Daily for 5 consecutive days in empty stomach orally. One adult dose is 4 globules of no. 20 medicated globule. One child

Sponsors

Ministry of AYUSH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects testing positive for SARS CoV-2 by RT-PCR, presenting with no symptoms or mild symptoms. 2. Subjects who are ready to provide written/digital informed consent and who are willing to participate and follow the protocol requirements of the clinical study.

Exclusion criteria

Exclusion criteria: 1. Cases of COVID-19 with clinical severity ranging from moderate to critical. 2. Pregnant and lactating females. 3. Subjects having uncontrolled and unstable co morbidity. 4. Immunocompromised subjects or those taking any kind of immunosupressive therapy. 5. COVIC-19 positive cases participating as subjects in other COVID-19 clinical trails. 6. Subjects having past history of allergy to any medicine that is part of the Homoeopathic intervention. Other conditions, which in the opinion of the investigator, makes the patient unsuitable for enrollment or could interfere with his participation in, and completion of the protocol.

Design outcomes

Primary

MeasureTime frame
To assess the effectiveness of Homoeopathic medicine Eupatorium perfoliatum 30 C in preventing the progression of severity of the disease in the SARS-Cov-2 tested positive asymptomatic and mild cases of COVID-19.Timepoint: 3 month

Secondary

MeasureTime frame
1. To assess the changes in Quality of Life (QoL) of the subjects using WHO QOL-BREF scale. 2. To assess the safety of Eupatorium perfoliatum 30 C drug by observing for adverse events.Timepoint: 3 months

Countries

India

Contacts

Public ContactDr Tapan Nath

North Eastern Institute of Ayurveda and Homoeopathy (NEIAH)

tapanbngn@gmail.com8837349308

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026