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TO SEE EFFECT OF PATHA CHURNA TABLETS IN FEMALES HAVING YONI KANDU

Randomized controlled clinical trial of patha churna vati in yoni kandu in kaphaj yonivyapad wsr candidiasis - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/087722
Enrollment
80
Registered
2025-05-27
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N761- Subacute and chronic vaginitis

Interventions

None listed

Sponsors

Dr Gauri Vijay Magar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Yoni kandu Yoni strava Yonigat toda

Exclusion criteria

Exclusion criteria: Patients having excessive yoni toda Pregnant women Patients previously diagnosed with HIV HBSAG VDRL

Design outcomes

Primary

MeasureTime frame
Reduce symptoms of yoni kandu yoni strava and yonigat toda within 7 days of start of treatmentTimepoint: 7 days

Secondary

MeasureTime frame
No recurrence of yoni kanduTimepoint: 21 days

Countries

India

Contacts

Public ContactDr Varsha Suresh Deshmukh

Shree Saptashrungi ayurved mahavidyalay and hospital Kamalnagar Hirawadi Panchavati Nashik

varshasdeshmukh15@gmail.com9403513983

Outcome results

None listed

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