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Comparing the effectiveness of Bhumyamalaki and Amalaki seed powders in managing symptoms of white discharge

Comparative clinical trial to determine the effect of Bhumyamalaki Churna and Amalaki Beej Churna in the Management of Shwetapradar W.S.R to Leucorrhoea - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106043
Enrollment
76
Registered
2026-03-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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 Komal Anil Gaikwad
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Married female patients within the reproductive age group. 2)Clinically diagnosed cases of Shwetapradar (leucorrhoea) based on classical Ayurvedic signs and symptoms, including- a)Yoni Srava (vaginal discharge) b)Yoni Kandu (itching) c)Yoni Daurgandhya (foul odor)

Exclusion criteria

Exclusion criteria: 1)Pregnant or lactating women 2)Women using intrauterine devices (IUDs) 3)Patients diagnosed with: Uterine polyps, Pelvic Inflammatory Disease (PID), Sexually Transmitted Infections (STIs), Uterine prolapse, Known cases of gynecological malignancies 4)Patients with systemic disorders such as: Diabetes Mellitus (DM) Hypertension (HTN), Moderate to severe anemia. 5)Any other chronic systemic illness that may interfere with the course of treatment or outcome evaluation

Design outcomes

Primary

MeasureTime frame
Reduction in sign and symptoms of Shwetpradar such as vaginal discharge, itching & backpainTimepoint: Duration of study: 18 Months. Duration of Treatment : 28 days Follow up: 7th, 14th, 21nd, and 28th day of treatment.

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactDr Amit shinde

Sst ayurved mahavidyalaya sangamner

amitshinde112@gmail.com9881303593

Outcome results

None listed

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