None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Subjects of high risk population. 2. Male or female subjects above the age of 03 years to 65 years. 3. Subject 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. Pregnant and Lactating woman. 2. Subjects having any medical or surgical condition that would require immediate medical or surgical intervention at the time of screening. 3. Subjects who are on any other regular medication( Alternative/ Modern)for any other ailments. 4. Subjects participating in any other clinical study or having participated in any other study one month prior to screening in the present study. 5. Subjects having a past history of allergy to any medicine that is part of the Homoeopathic intervention. Other conditions, which in the opinion of the investigators, makes the patient unsuitable for enrolment or could interfere with his participation in, and completion of the protocol.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess of occurrence of COVID-19 infection in healthy volunteers exposed to COVID-19 in the communityTimepoint: 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To assess the immunity status of the participants taking Arsenicum album -30 C 2. To evaluate the occurance of advarse event for safety assessment of Arsenicum album-30C.Timepoint: 6 months | — |
Countries
India
Contacts
North Eastern Institute of Ayurveda and Homoeopathy (NEIAH)