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Use of Panchavalkala Sneha Pichu in the management of Upapluta Yonivyapada (Leucorrhoea)

Clinical study to evaluate the role of Panchavalkala Sneha Pichu in the management of Upapluta Yonivyapada w.s.r to Leucorrhoea - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/086612
Enrollment
40
Registered
2025-05-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Health Condition 1: N898- Other specified noninflammatory disorders of vagina

Interventions

None listed

Sponsors

Dr Akshita Gangwar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Women in the age group of 18-45 years Patients complaining of white discharge with pricking pain per vagina as a cardinal symptom Patients willing for trial and ready to give written consent

Exclusion criteria

Exclusion criteria: Unmarried women. Patients suffering from STD s Any other major systemic disorder like Diabetes Mellitus, HTN, Thyroid Patient with any pelvic palpable pathology like cyst, fibroid etc

Design outcomes

Primary

MeasureTime frame
Improvement in amount of vaginal dischargeTimepoint: 3 months The drug trial will be given for 3 months and follow up will be done after cessation of medicine in 4th month

Secondary

MeasureTime frame
Relief in Itching,pain per vaginal & lower backacheTimepoint: After analyzing all the parameters the result will be assessed on the basis of symptomatic relief and improvement. Partially improvement after 1 month-patient get 40-60 percent relief from sign & symptoms Improvement after 2 month patient get 60-80 percent relief from sign & symptoms Cured after 3 month-patient get 80-100 percent relief from sign & symptoms.

Countries

India

Contacts

Public ContactDr Rama Khatavkar

Vaidya Yagya Dutt Sharma Ayurved Mahavidyalaya Khurja Bulandshahr

drbhapilsharma@gmail.com7018687930

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026