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Standard of care with homoeopathy as adjuvant in COVID19

Homeopathy as adjuvant to standard treatment protocol in management of corona virus infection- a randomized, placebo controlled, open label study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/10/028279
Enrollment
128
Registered
2020-10-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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: Homoeopathic medicines: A detailed history and examination will be gathered from the already available information of the patient in the admission records at hospital. The patients rand

Sponsors

Central Council for Research in Homeopathy Ministry Ministry of Ayush
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age > 18 years 2. All sexes 3. Case definitions for inclusion in the study will include moderate and severe cases as defined in the Guidance on appropriate treatment of suspect/confirmed case of COVID19 issued by Ministry of Health and Family Welfare, Govt of India on 07 Apr 2020. a. Moderate: Pneumonia with no signs of severe disease (Respiratory Rate 15 to 30/minute, SpO2 90%-94%). b. Severe: Severe Pneumonia (with respiratory rate 4. Laboratory confirmed SARS CoV-2 infection within last 10 days or SARS 5. CoV-2 test result pending with a high clinical suspicion as defined by: a. Cough of b. Bilateral pulmonary infiltrates on chest X Ray / CT scan or new hypoxaemia defined as SpO2 c. No alternative explanation for respiratory symptoms d. Scheduled for admission or enrolled within 48h of hospital admission

Exclusion criteria

Exclusion criteria: 1. Children 2. Covid Positive patients with severe co-morbidities 3. Pregnant and lactating women, infants and neonates 4. Not willing to give consent for adjuvant treatment 5. Inability to be contacted on D14 for clinical outcome assessment (unless died in hospital) 6. In the opinion of the clinical team, progression to death is imminent and inevitable within the next 24 hours, irrespective of the provision of treatments. 7. Symptoms of acute respiratory tract infection for > 10d before randomisation, and covid status unknown 8. Death within 24 Hrs. of admission

Design outcomes

Primary

MeasureTime frame
To compare duration required for change in disease status (from COVID positive to negative) in patients receiving adjuvant homoeopathic intervention with those receiving conventional treatment as institutional management protocol (IMP) in COVID-19 patients, categorized into moderate to severe stage of the diseaseTimepoint: To compare duration required for change in disease status (from COVID positive to negative) in patients receiving adjuvant homoeopathic intervention with those receiving conventional treatment as institutional management protocol (IMP) in COVID-19 patients, categorized into moderate to severe stage of the disease

Secondary

MeasureTime frame
To assess overall symptomatic relief to patients through MYMOP2 scaleTimepoint: 3 Months

Countries

India

Contacts

Public ContactDr Sushma Bhatnagar

All India Institute of Medical Sciences (AIIMS)

sushmabhatnagar1@gmail.com01129575209

Outcome results

None listed

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