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A randomized clinical trail of Mochras Varti (vaginal pessary ) in white discharge

A randomized control clinical trial to evaluate the effect of Mochras Varti in management of pathological leucorrhoea - NIl

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/102136
Enrollment
66
Registered
2026-01-27
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: N899- Noninflammatory disorder of vagina, unspecified Health Condition 2: N899- Noninflammatory disorder of vagina, unspecified Health Condition 3: N899- Noninflammatory disorder of vagina, unspecified

Interventions

None listed

Sponsors

Dr Rajshree patond
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients complaining of excessive vaginal discharge, lower abdominal Pain , backache. Vaginal itching, offensive discharge with or without smell.

Exclusion criteria

Exclusion criteria: Patient with DM, Hepatic, Renal and Cardiac disease. Patient with HIV, VDRL, HBsAG, STDs. Neoplasm (cervical and uterine malignancy). Female in puerperium period and Pregnant women. Patient with psychosomatic diseases. Any other systemic diseases

Design outcomes

Primary

MeasureTime frame
To evaluate the effect of MOCHRAS VARTI in management of Pathological leucorrhoea.Timepoint: 1 week

Secondary

MeasureTime frame
1.To observe the effect of Mochras varti in discharge of Pathological leucorrhoea. 2.To observe the effect of Mochras varti on odour in Pathological leucorrhoea. 3. To observe the effect of Mochras varti on itching in Pathological leucorrhoea. 4. To asses the improvement by parameters like pain scale. 5. To asses the causative organisms presence or absence.Timepoint: 1 week

Countries

India

Contacts

Public ContactDr Amrita Mishra

R.A.Podar medical Ayurveda college Worli

dramritamishra@gmail.com9823171494

Outcome results

None listed

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