Use of Karpasa Moola (Cotton plant roots in the management of Shweta Pradara (Leucorrhoea)

Clinical Study To Evaluate The Efficacy Of Karpasa Moola In The Management Of Shweta Pradar w.s.r. To Leucorrhoea - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/04/108958

Enrollment

Registered

2026-04-21

Start date

Unknown

Completion date

Unknown

Last updated

2026-04-27

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.. 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,HTN etc. Patients having any other gynecological problems like prolapse and fibroid uterus etc. Pregnant women with profuse white discharge.

Design outcomes

Primary

Measure	Time frame
Improvement in amount of vaginal dischargeTimepoint: 2 months The drug trial will be given for 2 months and follow up will be done after cessation of medicine in 3rd month	—

Secondary

Measure	Time frame
Relief in itching, pain, odour per vaginal & Lower backacheTimepoint: After analysing all the parameters the result will be assessed on the basis of symptomatic relief and improvement. Partially improvement after 7 days patient get 40-60 percent from sign & symptoms improvement after 15 days patient get 60-80 percent relief from sign & symptoms Cured after 2 months patients get 80- 100 percent relief from sign &symptoms	—

Measure

Time frame

Relief in itching, pain, odour per vaginal & Lower backacheTimepoint: After analysing all the parameters the result will be assessed on the basis of symptomatic relief and improvement. Partially improvement after 7 days patient get 40-60 percent from sign & symptoms improvement after 15 days patient get 60-80 percent relief from sign & symptoms Cured after 2 months patients get 80- 100 percent relief from sign &symptoms

—

Countries

India

Contacts

Public ContactDr Bhappil Sharma

Vaidya Yagya Dutt Sharma Ayurved Mahavidyalaya Khurja

drbhapilsharma@gmail.com7018687930

Outcome results