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Clinical trial on COVID 19 patients to Improve Immunity

â??A Prospective, Open label, Randomized-controlled study to evaluate the efficacy and safety of Herbovir Syrup in mildly symptomatic COVID- 19 patientsâ??

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/08/027041
Enrollment
40
Registered
2020-08-09
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

Interventions

Intervention1: HERBOVIR SYRUP (Ayush approved formulation): Dose: 10 ml thrice daily Dosage form: Syrup Route: Orally Time of Administration: Morning,After noon and night after meal Total duration:

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 are willing to give consent to the study 3.COVID-19 positive clinical symptoms and (subsequently) confirmedby the current recommended confirmatory test. 4.Mild to moderate clinical disease 5.Can take oral medicines 6.Subject willing to abide by and comply with the study protocol

Exclusion criteria

Exclusion criteria: 1.Age less than 18 years and more than 65 years 2.Pregnancy and lactation 3.Severe or complicated course of COVID-19 disease 4.Presence of acute hypoxic respiratory failure/ need for Intensive care unit (ICU) stay/Patients who need mechanical ventilation. 5.Subjects taking steroid treatment and or any kind ofimmunosuppressive therapy 6.Any uncontrolled systemic disease, infection 7.Those with serious Cardiovascular, Cerebrovascular, Respiratory, Liver or Renal disease or any other disorder. 8.Other conditions, which in the opinion of the investigators makes the patient unsuitable for enrolment or could interfere in adherence to of the study protocol

Design outcomes

Primary

MeasureTime frame
Improvement in LDH, TLC, CRP, D-DIMER and RT PCR from baseline to end of the studyTimepoint: Day 0 and End of the study (Day 7 to 14)

Secondary

MeasureTime frame
1.Adverse events (AEs), frequency and severity 2.Number of subjects who discontinue study due to adverse events 3.Changes in vital parameters and safety laboratory parameters Timepoint: Day 0 and Day 14

Countries

India

Contacts

Public ContactSri H Srinivas

Venkat Pharma

sreenivas.drugs@gmail.com9448080317

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 16, 2026