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A Clinical Study to see the effect of Haritaki kwatha Yonidhawan and Haritaki taila Pichu in Kaphaj Yonivyapad.

Single Arm Open Label Clinical Study to Evaluate the Effect of Haritaki Kwatha Yonidhawan along with Haritaki Taila Pichu in Kaphaj Yonivyapad.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/08/035937
Enrollment
30
Registered
2021-08-26
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: N761- Subacute and chronic vaginitis

Interventions

Intervention1: Haritaki Kwatha Yonidhawan: Half litre Haritaki Kwatha will be used for Yoni Dhawan for duration of 6 days Intervention2: Haritaki Taila Pichu: Haritaki Taila Pichu will be Kept per vag

Sponsors

Dr Ekta Vijay Deshmukh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: MARRIED WOMEN WITH KAPHAJ YONIVYAD WITH CLINICAL FEATURES OF KANDU, SHWETA-SHEET PICCHIL ARTAVA STRAV AND ALPA VEDANA

Exclusion criteria

Exclusion criteria: Pregnancy Drug Allergy Systematic Diseases Like TB , STD PV Bleeding Malignant Diseases of Genital Tract.

Design outcomes

Primary

MeasureTime frame
TO Evaluate the Effect of Haritaki Kwatha Yonidhawan along with Haritaki Taila Pichu in Kaphaj Yoni Vyapad.Timepoint: 6 days—

Secondary

MeasureTime frame
To Study any adverse effect of Haritaki Kwatha Yonidhawan Along With Haritaki Taila Pichu in Kaphaj Yonivyapad.Timepoint: During the Study Period.—

Countries

India

Contacts

Public ContactDr Kalpana B Ayare

Sumatibhai Shah Ayurved College

drkalpanaayare@gmail.com9423295630

Outcome results

None listed

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