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Study to evaluate the effect of two herbal drugs NIFAy.C-19(CONTAZAP)and AYUSH 64 in corona patients.

Clinical study to evaluate the efficacy of NIFAy.C-19 (CONTAZAP) in mild to moderate COVID-19 positive patients: A randomized open label parallel group study.

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/01/030169
Enrollment
120
Registered
2021-01-01
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: Cap.NIFAy.C19(CONTAZAP)-640 mg a polyherbal formulation: The composition of NIFAy.C-19 (CONTAZAP) includes aqueous extract of Kalmegh (Andrographis panniculata Nees), Revand Chini (Rheu

Sponsors

National Innovation FoundationIndia
Lead Sponsor
Central Council of Research in Ayurvedic Sciences
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients tested positive for SARS-CoV2 virus infection 2.Patients having one or more symptoms of mild to moderate category of COVID-19 infection. 3 Patients of either sex. 4.Age: 18 years to 80 years. 5.Patients who can take oral medicines 6.Patients who are ready to give consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1.Patients having severe symptoms of COVID-19 infection. 2.Age below 18 years and more than 80 years. 3.Patients requiring intubation or mechanical ventilators. 4.Pregnant and lactating women. 5.Oncological disease and other systematic un-controlled condition 6.RFT >= 2.5 times of the upper limit. 7.Patients participating in other trial

Design outcomes

Primary

MeasureTime frame
a) Mean time (days) for clinical recovery as per clinical recovery criteria. b) Number of patients showing â??clinical recoveryâ?? Timepoint: a) at baseline, 8th day, 14th day, 21st day (if required) showing â??clinical recoveryâ??

Secondary

MeasureTime frame
1.Percentage of patients with negative SARS-CoV-2 on nasal or throat swab in a 2 days continuous RT-PCR test. 2.Improvement in selected laboratory Parameters: CBC, RBS, ESR, Hs-CRP, LDH,S.Ferritin, IL-6, LFT and RFT. 3.No of cases Reporting any ADR/AE 4. Number of participants referred with onset of complications. Timepoint: Baseline- 8 days 15 days

Countries

India

Contacts

Public ContactDr N R Singh

Ch. Brahm Prakash Ayurved Charak Sansthan

naimishraj@yahoo.com9560659728

Outcome results

None listed

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