The study comparing two kashaya for relieving vulvar itching in females.

A comparative clinical study to evaluate the efficacy of Kanduhar mahakashaya and Sarivadi Kashaya in the management of Acharana yonivyapad W.S.R pruritis vulva - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/05/111118

Enrollment

Registered

2026-05-26

Start date

Unknown

Completion date

Unknown

Last updated

2026-06-01

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

Conditions

Health Condition 1: N908- Other specified noninflammatory disorders of vulva and perineum

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients presenting with lakshana of Acharana yonivyapad having Kandu , Srava, daurgandhya

Exclusion criteria

Exclusion criteria: patients after menopause, willing to conceive, patients of uterine prolapse and Ca cervix, on oral contraceptives or using intrauterine contraceptive devices, with Diabetes mellitus, tuberculosis, jaundice, severe HT, with extensive chronic cervicitis, fibroid and malignancy, VDRL,HIV, HBsAg positive patient, herpes, HPV positive patients, pregnant and lactating women

Design outcomes

Primary

Measure	Time frame
Reduction in severity of vulvar itching(kandu) assessed by grading scoreTimepoint: 30 days Trial drug is given for 30 days with anupana and follow up will be done after every 7 days	—

Secondary

Measure	Time frame
Improvement in Kandu, srava and daurgandhya after every 7 daysTimepoint: 30 days	—

Countries

India

Contacts

Public ContactDr Mamata Kumari swain

Jeevan jyoti ayurvedic medical college and hospital Aligarh

swaindrmamata@gmail.com9348576189

Outcome results