Vaginitis

Clinical study to evaluate the efficacy of bruhatyadi yonivarti in kaphaj yonivyapad w.s.r. to vulvo vaginal candidiasis

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/03/012376

Enrollment

Registered

2018-03-06

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- KAPHAJ YONIVYAPAD/VULVOVAGINAL CANDIDIASIS

Interventions

Intervention1: BRUHATYADI VARTI: 1) SOLANUM XANTHOCARPUM 2) CURCUMA LONGA 3) BERBERIS ARISTATA ( 1 varti at bed time for 7 days (vaginally)) Control Intervention1: PIPPALYADI VARTI: 1) PIPER LONGUM 2)

Eligibility

Inclusion criteria

Inclusion criteria: 1- Married Women 2-Yonitaha Picchilla Srava (thick, greenish-yellowish & frothy discharge) 3-Yonikandu (itching) 4-Alpavedana (mild Pain) 5-Katishula (backache)

Exclusion criteria

Exclusion criteria: 1-Unmarried 2-Post menopausal 3-Uterine fibroid 4-Cervical erosion 5-Pregnancy 6-Patients with any IUDs 7-Other sexually Transmitted disease 8-Diabetes mellitus 9-HIV 10-Patients having age group of above 45 years and below 18 years

Design outcomes

Primary

Measure	Time frame
REDUSES YONITAHA PICCHILL SRAVA, YONIKANDU, ALPAVEDANA (DULL PAIN IN VAGINA)Timepoint: 14-21 DAYS	—

Secondary

Measure	Time frame
REDUCED THICK WHITE CHEESY DISCHARGE, REDUCED VAGINAL WALL INFLAMMATIONTimepoint: 14-21 DAYS	—

Countries

India

Contacts

Public ContactDr Mansi Modi

Parul University

mansi.modi1@gmail.com9979883317

Outcome results

None listed

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