Skip to content

Clinical trial on Ayurvedic product for viral and bacterial infections

A prospective, single arm, multicentric clinical study to evaluate the safety and efficacy of HERBOVIR syrup in subjects with upper respiratory tract infection along with standard of care

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/07/026434
Enrollment
40
Registered
2020-07-08
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: J205- Acute bronchitis due to respiratory syncytial virus

Interventions

Intervention1: HERBOVIR Syrup: Dose : 10 ml of HERBOVIR syrup three times daily in the morning (After Breakfast), after noon (Post lunch) and in night after dinner Route: Orally Duration: Three time

Sponsors

VENKAT PHARMA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects aged 18-65 years of age and of either sex 2. subjects who were disposed to give consent to the study and willing for follow-up 3. Subjects who are willing to sign ICF 4. Clinical signs and symptoms of an URTI with a duration of up to 24 hours accompanied with or without fever 37.5 C (axillary body temperature) or higher 5. At least 1 of 3 types of URTI symptoms â?? Nasal (plugged nose, runny nose, sneezing), Pharyngeal (scratchy throat, sore throat, pharyngeal hyperaemia), Cough (ordinary cough without suspicion of acute lower respiratory tract disease). At least 1 of 5 general symptoms â?? feeling tired, weakness, body ache, irritable or whiney,or less active 6. Not be in need of hospitalized medical care at screening

Exclusion criteria

Exclusion criteria: 1. Age less than 18 years and more than 65 years 2. Pregnancy 3. Severe or complicated course of URTI. 4. Signs of acute lower respiratory tract disease. 5. Daily use of antibiotics, steroids and cytotoxic agents. 6. Any uncontrolled systemic disease, infection 7. Those with serious Cardiovascular, Cerebrovascular, Respiratory, Liver or Renal disease• or any other disorder

Design outcomes

Primary

MeasureTime frame
Change from baseline in the Wisconsin Upper Respiratory Symptom SurveyTimepoint: Day 0 to Day 7

Secondary

MeasureTime frame
â?¢ Adverse events (AEs), â?¢ frequency and severity Number of subjects who discontinue study due to adverse events â?¢ Changes in vital parameters and laboratory investigations. Timepoint: Day 0 to Day 7

Countries

India

Contacts

Public ContactSri HSrinivas

Venkat Pharma

sreenivas.drugs@gmail.com9448080317

Outcome results

None listed

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