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A study to evaluate the effect of Udumbara Kashaya Yoni Prakshalana in Vaginitis

A Randomized Open-Labelled Controlled Clinical Study To Evaluate The Efficacy Of Udumbara Kashaya Yoni Prakshalana In Shweta Pradara w.s.r To Vaginitis. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/055880
Enrollment
30
Registered
2023-07-31
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Health Condition 1: N768- Other specified inflammation of vagina and vulva Health Condition 2: N768- Other specified inflammation of vagina and vulva

Interventions

None listed

Sponsors

Dr AFREEN KOUSAR ALI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects between the age group of 20-40 years. 2. Subjects willing for Per speculum and Per vaginal examination. 3. Married woman. 4. Subjects presenting classical symptoms of Shwetha Pradara. 5. Subjects with the classical symptoms of Vaginitis. 6. Subjects willing to sign the consent form.

Exclusion criteria

Exclusion criteria: 1. Unmarried women. 2. Women below 20 years and above 40 years. 3. Pregnant woman. 4. Subject with known case of Benign and Malignant tumors. 5. Subject with known case of PID. 6. Subject with known case of Cervicitis. 7. Subject with known case of Systemic disorders. 8. Subject with known case of STDs (Syphilis, Chlamydia, Gonorrhea).

Design outcomes

Primary

MeasureTime frame
Complete reduction in white discahrgeTimepoint: Before treatment 0th day After treatment 7th day Follow up 15th day

Secondary

MeasureTime frame
Reduction in itching, burning micturition, backache, foul smell in dischargeTimepoint: Before treatment 0th day After treatment 7th day Follow up 15th day

Countries

India

Contacts

Public ContactDr Rajani Kagga

Sri Sri College Of Ayurvedic Science And Research Hospital

drcrajanii@gmail.com9739766448

Outcome results

None listed

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