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To see the effect of Yoni varti in the management of vaginal discharge w.s.r to Vulvovaginal candidiasis.

A Comparative Study to Assess the Efficacy of Lodhradi Yonivarti and Vaginal Tablet in the Management of Kaphaja Yoni vyapada w.s.r. to Vulvovaginal Candidiasis. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/071898
Enrollment
60
Registered
2024-08-05
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: N760- Acute vaginitis

Interventions

None listed

Sponsors

Priyanka
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patient willing to participate in the trial 2)Married women 3)Age- 20 years-50 years 4)Microscopically positive for Pseudo hyphae. 5)Patient complaining of any two from: . Yoni srava (vaginal discharge) . Yoni kandu (itching) . Alpa vedana (inguinal pain and backache) . Yoni durgandh (smell in yoni)

Exclusion criteria

Exclusion criteria: 1)Patient not willing to participate in the trial 2)Unmarried women and Pregnant women 3)Age less than 20 years and more than 50 years 4)Patient with known case of pelvic pathology 5)known case of sexually transmitted diseases like VDRL HIV GONORRHEA 6)Diagnosed systemic illness like asthma Tuberculosis Malignancy etc

Design outcomes

Primary

MeasureTime frame
(1) To observe the efficacy of Lodhradi Yonivarti in Kaphaj Yonivyapad W.S.R Vulvovaginal Candidiasis. Parameters include vaginal discharge, pain, colour of discharge, itching, consistency of discharge, smell in discharge and wet vaginal smear.Timepoint: Follow up in each cycle after completion of procedure for subjective parameters and 15 days after completion of procedure for objective parameters.

Secondary

MeasureTime frame
To help a woman to get relief from the symptoms & live a healthy life.Timepoint: Follow up in each cycle after completion of procedure for subjective parameters & 15 days after completion of procedure for objective parameters.

Countries

India

Contacts

Public ContactDr.Priyanka

Institute for ayurved studies and research,SKAU,kurukshetra

Drsunititanwar@gmail.com9996311778

Outcome results

None listed

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