Role of Bruhtyadi Choorna Yonidhoopan in Yonikandu w.s.r. Vulvovaginal candidiasis in comparison with Candid ointment

A Randomised Controlled study to assess the effectiveness of Bruhtyadi Choorna Yonidhoopan in comparison with Candid ointment in Yonikandu in Kaphaj Yonivyapad w.s.r. Vulvovaginal Candidiasis. - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/03/063704

Enrollment

Registered

2024-03-06

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-01

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

Conditions

Health Condition 1: B373- Candidiasis of vulva and vagina

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients under reproductive age group of 25-35 years. 2. Patients complaining of Yonikandu (Vaginal Itching). 3. Womens who are sexually active. 4. Patients with complaints of yonikandu for less than 15 days.

Exclusion criteria

Exclusion criteria: 1. Patients in menstrual bleeding phase. 2. Patient with Chronic PID. 3. Patient with genital malignancy. 4. Under prolonged use of antibiotics.

Design outcomes

Primary

Measure	Time frame
To study the effectiveness of Bruhtyadi Choorna Yonidhoopan in Yonikandu in Kaphaj Yonivyapad.Timepoint: The study will be conducted for 10 days follow up on day 1,day 7, day 14.	—

Secondary

Measure	Time frame
1.Establish the best possible comparison of yonikandu with vulvovaginal candidiasis. 2.For Validation of treatment given in ayurvedic granthas.Timepoint: The study will be conducted for 10 days follow up on day 1,day 7, day 14	—

Countries

India

Contacts

Public ContactDr Bhagyashri Satish Salunkhe

Dr. G.D.Pol Foundation, YMT Ayurvedic Medical College, Kharghar

seema.mehre@gmail.com9930940403

Outcome results