Use of Rohitaka Moola Kalka and Amalaki beeja kalka in the management of Shweta Pradara (Leucorrhoea)

Comparative Clinical Study To Evaluate The Efficacy Of Rohitaka Moola Kalka & Amalaki Beeja Kalka In The Management Of Shweta Pradara w s.r. To Leucorrhoea - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/086583

Enrollment

Registered

2025-05-08

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

Eligibility

Inclusion criteria

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

Exclusion criteria

Exclusion criteria: Patients suffering from STD s Any other systemic disorder like Diabetes Mellitus Patients having any other gynecological problems like prolapse, fibroid, etc Pregnant women with profuse white discharge

Design outcomes

Primary

Measure	Time frame
Improvement in amount of vaginal dischargeTimepoint: 3 months The trial drug will be given for 3 months with anupana and follow up will be done after cessation of medicine in 4 month	—

Secondary

Measure	Time frame
Relief in Itching Lower backache and tenderness Per vaginaTimepoint: After analyzing all the parameters the result will be assessed on the basis of symptomatic relief and improvement. Partially improvement after 3 days- patient get 30 percent relief from sign and symptoms Improvement after 1 month Patient get 40-50 percent relief from sign and symptoms Improvement after 2 month patient get 60-80 percent relief from sign and symptoms Cured after 3 month pateint get 80-100 percent relief from sign and symptoms.	—

Measure

Time frame

Relief in Itching Lower backache and tenderness Per vaginaTimepoint: After analyzing all the parameters the result will be assessed on the basis of symptomatic relief and improvement. Partially improvement after 3 days- patient get 30 percent relief from sign and symptoms Improvement after 1 month Patient get 40-50 percent relief from sign and symptoms Improvement after 2 month patient get 60-80 percent relief from sign and symptoms Cured after 3 month pateint get 80-100 percent relief from sign and symptoms.

—

Countries

India

Contacts

Public ContactDr Rama Khatavkar

Vaidya Yagya Dutt Sharma Ayurved Mahavidyalaya

drbhapilsharma@gmail.com7018687930

Outcome results