A Clinical Study To Evaluate The Efficacy Of Aragvadhadi Kwath Yonidhavan In Kaphaj Yonivyapad With Special Reference To Vulvovaginal Candidiasis

An Open Randomized Control Clinical Trial TO Evaluate The Efficacy Of Aragvadhadi Kwath Yonidhavan In Kaphaj Yonivyapad With Special Reference To Vulvovaginal Candidiasis - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/02/104229

Enrollment

Registered

2026-02-18

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

Health Condition 1: N771- Vaginitis, vulvitis and vulvovaginitis in diseases classified elsewhere Health Condition 2: N771- Vaginitis, vulvitis and vulvovaginitis in diseases classified elsewhere

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Married Patients having Kaphaj Yonivyapad i.e having following signs and symptoms 2. Yonigata shweta picchil strav, Yoni kandu Yonigat alpavedana 3. Patient selection of vaginal candidiasis will be confirmed after doing KOH Test

Exclusion criteria

Exclusion criteria: 1. Unmarried female patients. 2. Known cases of sexually transmitted diseases. 3. Uncontrolled DM & HTN. 4. Pregnant women. 5. Cervical polyp and cervical erosion. 6. Patients with intolerable severe pain (VAS scale of 8 to 10) will be excluded.

Design outcomes

Primary

Measure	Time frame
Aragvadhadi kwath yonidhavan is effective in Kaphaj Yonivyapad w.s.r.to VulvoVaginal candidiasis.Timepoint: 7 days	—

Secondary

Measure	Time frame
1. Aragvadhadi kwath yonidhavan for 7 days increases pH of vaginaTimepoint: Follow up 1st 3rd 7th day during treatment	—

Countries

India

Contacts

Public ContactDr Dilip Vitthal Katare

Hon Shri Annasaheb Dange Ayurved Medical College Post Graduate and Research Centre Ashta

drdilipkatareashta@gmail.com9881215521

Outcome results