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To evaluate the efficacy of Leucronil tablets in the patients suffering from white discharge per vagina

Effect of Leucronil® tablets in the patients with Leucorrhea: An open clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/02/005515
Enrollment
30
Registered
2015-02-09
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N80-N98- Noninflammatory disorders of female genital tract Health Condition 2: null- patients suffering from Leucorrhea

Interventions

Intervention1: Tab Lucronil : Ashwagandha Extract (Withania somnifera 40 mg Vidari Extract (Pueraria tuberosa)20 mg Badi Elaichi Extract (Amomum subulatum)30 mg Ashok Chhal Extract (Saraca indica) 4

Sponsors

yurvedic Research Foundation Pvt ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Married females of Age group 20 to 40 years having leucorrhoea due to non-infective cervical lesions e.g. cervical erosion, chronic cervicitis, mucous polyps, increased pelvic congestion e.g. uterine prolapsed, acquired retroverted uterus, chronic pelvic inflammation Controlled diabetes

Exclusion criteria

Exclusion criteria: i. Pregnant or lactating women ii. Patients on Oral Contraceptive Pills iii. Patients with IUCD iv. Patients with physiological leucorrhoea (e.g. during ovulation, pre-menstrual, pregnancy) v. Patients with abnormal (excessive) vaginal discharge due to neoplasmic changes vi. Positive history of venereal diseases vii. Patients suffering from uncontrolled diabetes viii. Patients with Anemia (Hb% below 7)

Design outcomes

Primary

MeasureTime frame
The outcomes of the study will be measured in terms of clinical signs - per vaginal examination and symptoms Pap smear test microbiological improvement. Timepoint: Every 15 days for a period of one month

Secondary

MeasureTime frame
To evaluate the safety and tolerability of the formulation in patientsa suffering from LeucorrheaTimepoint: Every 15 days

Countries

India

Contacts

Public ContactDr Supriya Bhalerao

Interactive Research School for Health Affairs

supriya.bhalerao@gmail.com9869555272

Outcome results

None listed

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