Skip to content

Herbal Steaminhaler clinical trial on COVID patients

A Prospective, Open Label, multi Center clinical Study to evaluate the Safety, Efficacy And Tolerability Of AZADVIR (Herbal Steaminhaler) In Asymptomatic, Mildly Symptomatic COVID -19 Patients And Health Care Workers Posted To Covid Wards

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/06/026181
Enrollment
40
Registered
2020-06-26
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 Health Condition 2: B342- Coronavirus infection, unspecified

Interventions

Intervention1: AZADVIR Drops : Herbal steam inhaler: Two drops in steam inhaler Twice daily Morning and Evening Duration : Day 0 to Day 7 Control Intervention1: NIL: NIL

Sponsors

HAOMA WELLNESS CENTER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male or non-pregnant female adult with or without comorbidities between the agre group of 18-85 years of age at time of enrollment 2. Has laboratory-confirmed positive COVID-19 infection as determined by RT-PCR or other commercial or public health assay in any specimen, an RT-PCR (Nasopharynx, Throat, and Blood) test shall be repeated to assess eligibility 3. Subject (or legally authorized representative) provides written informed consent prior to initiation of any study procedures 4. Health care workers who visited to COVID patients

Exclusion criteria

Exclusion criteria: 1. Testing positive for HIV, HbsAg, HCV infection, VDRL. 2. Females who are currently pregnant or breastfeeding. 3. Allergy or other contraindication to one of the investigational products. 4. Has received Eflornithine within the last 10 days. 5. Has received anti-viral, anti-malarial or anti-bacterial within the last 14 days. 6. Alanine Aminotransferase (ALT) or aspartate aminotransferase (AST) > 5 X upper limit of normal (ULN). 7. QTc interval >= 500ms. 8. Recent Myocardial Infarction (within last 6 months). 9. Known case of (K/C/O) Congestive heart failure. 10. K/C/O Chronic Kidney Disease. 11. K/C/O active Tuberculosis. 12. History of drug or alcohol dependence in the past 6 months. 13. 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. 14. Anticipated transfer to another hospital which is not a study site within 72 hours. 15. K/C/O of epilepsy or CNS disorders.

Design outcomes

Primary

MeasureTime frame
To evaluate the efficacy AZADVIR (Herbal steamInhaler) supplement in COVID-19 patients Expecting 5 to 7 days RT PCR COVID negative testTimepoint: Day 0 to Day 10

Secondary

MeasureTime frame
â?¢ To assess the organoleptic properties of AZADVIR (Herbal steamInhaler) through a feedback questionnaireTimepoint: Day 0, Day 5 and Day 10

Countries

India

Contacts

Public ContactKavya Kannoth Shaji

HAOMA WELLNESS CENTER

drshajikannoth@gmail.com8048664855

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 15, 2026