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A clinical study to evaluate the efficacy of nishadikwathaghanavati and brihatsindooradyam tailam in vicharchika

To evaluate the efficacy of nishadikwathaghanavati and brihatsindooradyam tailam in vicharchika - a clinical study

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/06/014576
Enrollment
90
Registered
2018-06-19
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: null- diagnosed or undiagnosed case of vicharchika

Interventions

Intervention1: brihatsindooradyam tailam, nishadi kwathaghana vati , brihatsindooradyam tailam and nishadi kwathaghana vati: 3 groups are in present trial.in 1st,brihatsindooradyam tailam, in 2nd gro

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Classical sign & symptoms of vicharchika like kandu, pidika, srava, vaiyvarnya, daha, rukshata, vedana etc. Uncomplicated cases of vicharchika.

Exclusion criteria

Exclusion criteria: Age more than 60 year and below 18 years. person suffering with systemic diseases like DM, HTN,malignancy, TB, cardiac disorder VDRL+cases

Design outcomes

Primary

MeasureTime frame
trial drugs should cure vicharchika completelyTimepoint: trial drug should complete in two months

Secondary

MeasureTime frame
among three group which group will be betterTimepoint: trial drug should complete in two months

Countries

India

Contacts

Public ContactMadhu Pathak

National Institute of Ayurveda,Jaipur

dr.madhupathak81@gmail.com7877020139

Outcome results

None listed

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