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New homeopathic medicine for prevention of COVID-19 infection

Series of N-of-1 trials to detect the effects of ultra-diluted delta SARS-CoV-2 spike protein in expression of interferons in healthy human volunteers

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/11/038253
Enrollment
10
Registered
2021-11-25
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

None listed

Interventions

Intervention1: iAttos ââ?¬â?? Ultra-diluted delta SARS-CoV-2 spike protein receptor binding domain ââ?¬â?? 6cH potency: Intervention is planned as administering the investigational medicinal product

Sponsors

Heritage Institute of Technology Kolkata
Lead Sponsor
D N De Homoeopathic Medical College and Hospital
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 65 years 2. No major untreated diseases with apparently healthy status 3. No abnormality detected during clinical examination by experts and routine laboratory examinations (complete hemogram, fasting blood sugar, lipid profile, liver enzymes, urine for routine examination and microscopy, electrocardiogram, chest X-ray, ultrasonography of whole abdomen) 4. Literate patients; ability to read patient information sheet and voluntarily providing with written informed consent

Exclusion criteria

Exclusion criteria: 1. Vulnerable population ââ?¬â?? unconscious, ambulatory, too sick for consultation, differently abled, terminally or critically ill patients, mentally incompetent subjects 2. Diagnosed cases of unstable mental or psychiatric illness or other uncontrolled or life-threatening illness affecting quality of life or any organ failure 3. Pregnant and puerperal women, lactating mothers 4. Tobacco chewing and/or smoking, alcoholism, and/or any other form(s) of substance abuse and/or dependence 5. Self-reported immune-compromised state (e.g., HIV)

Design outcomes

Primary

MeasureTime frame
Interferon alpha, beta and gammaTimepoint: At baseline, after 48 and 72 hours, and after 7 days. The sequence will be repeated thrice after an intervening wash-out period of 7 days

Secondary

MeasureTime frame
Interleukin 1�², 6, 8, 10Timepoint: At baseline, after 48 and 72 hours, and after 7 days. The sequence will be repeated thrice after an intervening wash-out period of 7 days;Tumor growth factor �²1, �²3Timepoint: At baseline, after 48 and 72 hours, and after 7 days. The sequence will be repeated thrice after an intervening wash-out period of 7 days

Countries

India

Contacts

Public ContactProf Dr Subhasish Ganguly

D. N. De Homoeopathic Medical College and Hospital

dr.subhasish67@gmail.com9007263548

Outcome results

None listed

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