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A clinical study to evaluate the efficacy of Laghumalini vasant rasa in the management of Shweta Pradara with special reference to Abnormal vaginal discharge

A clinical study to evaluate the efficacy of Laghumalini vasant rasa in the management of Shweta pradara w.s.r. Abnormal vaginal discharge - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100589
Enrollment
40
Registered
2026-01-08
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Jeevan Jyoti Ayurvedic medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Women aged between 18-45 years. Patient having excessive whitish vaginal discharge with rule out pruritus along with other sign and symptoms of Shweta Pradara will be taken for study.

Exclusion criteria

Exclusion criteria: Women below 18 years and above 45 years PID Genital prolapse Systemic disorders Patient having metabolic disorders such as DM Hyperthyroidism Hypothyroidism Patient having blood stained discharge PATIENTS HAVING BLOOD STAINED DISCHARGE

Design outcomes

Primary

MeasureTime frame
Relief from yoni srava,yoni kandu,kati sula,yoni daha and yoni dourgandhaTimepoint: 3 months—

Secondary

MeasureTime frame
Improvement in quality of life reduction in associated symptoms such as Kati shoola, Maithun asahishnutaTimepoint: 3 months—

Countries

India

Contacts

Public ContactDr Mamata Kumari Swain

Jeevan Jyoti Ayurvedic medical college and hospital aligarh

swaindrmamata@gmail.com9348576189

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026