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Efficacy of Darvyadi Kashaya orally and Karanja Churna orally along with Karanja Ointment locally in the management of Kaphaj Yonivyapad

Randomized controlled clinical trial to evaluate the efficacy of Darvyadi Kashaya in the management of Kaphaj Yonivyapad - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088956
Enrollment
100
Registered
2025-06-16
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: N889- Noninflammatory disorder of cervixuteri, unspecified

Interventions

None listed

Sponsors

CSMSS Ayurved Mahavidyala and Rugnalaya Kanchanwadi Aurangabad Maharashtra India 431011
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Married women between 21-40 yrs 2.Non pregnant patients 3.Patients diagnosed with Kaphaj Yonivyapad with clinical features of Yonikandu,pandu,picchil strav and Alpavedana

Exclusion criteria

Exclusion criteria: 1.Unmarried 2.Antenatal and Postnatal patients 3.Veneral diseases , Diabetes 4.Suspected case of Ca Cervix 5.Patient with IUCD & on contraceptive pills 6.Pelvic Inflammatory Diseases [PID]

Design outcomes

Primary

MeasureTime frame
To study the effect of Darvyadi Kashaya in the management of Kaphaj YonivyapadTimepoint: Baseline - 4th,7th,15th day

Secondary

MeasureTime frame
1.To study Kaphaj Yonivyapad as per Ayurvedic view 2.To study Leucorrhea & vaginal health according to modern view 3.Any adverse effect of Darvyadi Kashaya in the Kaphaj Yonivyapad will be noted 4.To compare efficacy of Darvyadi Kashaya orally & Karanja churna orally along with Karanja ointment locally in the management of Kaphaj YonivyapadTimepoint: Baseline - 4th,7th,15th day

Countries

India

Contacts

Public ContactDr Sayali Anil Tambade

CSMSS Ayurved Mahavidyala and Rugnalaya Kanchanwadi Aurangabad

amolhavale@gmail.com9822538957

Outcome results

None listed

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