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CLINICAL EFFECT OF PUGAKHANDA AND AYUSH PVK GEL ON WHITE DISCHARGE

CLINICAL EVALUATION OF AYURVEDIC FORMULATIONS PUGAKHANDA AND AYUSH PVK GEL IN THE MANAGEMENT OF SWETAPRADARA (PATHOLOGICAL LEUCORRHOEA)

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/07/026626
Enrollment
40
Registered
2020-07-16
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: N948- Other specified conditions associated with female genital organs and menstrual cycle

Interventions

Intervention1: PUGAKHANDA AND AYUSH PVK Gel: Pugakhanda 10 gm twice a day after food with milk for two months AYUSH PVK Gel 3gm once daily applied intra vaginal for 15 days Control Intervention1:

Sponsors

CENTRAL COUNCIL FOR RESEARCH IN AYURVEDIC SCIENCES
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Married woman of age between 18 to 40 years. 2.Presence of discharge per vaginum with or without itching/burning sensation /dyspareunia /foul smell for at least one month. 3.Patient agrees to refrain from use of douches oral or intra-vaginal antibiotics or antifungal agents or lubricants during the entire study period. 4.Patient willing and agrees to participate for three months and signs informed consent.

Exclusion criteria

Exclusion criteria: 1)Patient with Pelvic Inflammatory Disease (PID). 2)Patient with Abnormal Papanicolaou smear with Intra-epithelial or invasive cancer. 3)Patient with unexplained vaginal bleeding. 4)Abnormal findings on pelvic Sonography. 5)Patient with positive pregnancy test. 6)Patient with Fibromyoma, polyp ovarian tumour or cyst prolapse. 7)Systemic disease like heart disease tuberculosis and uncontrolled Diabetes Mellitus Hypertension and Severe anemia i.e Hemoglobin less than 7 gms 8)Use of antibiotics or local vaginal formulation within the previous month 9)Endocervical smear positive for gonococci, or positive VDRL HIV & HbsAg test 10)Patients who are currently participating in any other clinical trial or participated in past four weeks.

Design outcomes

Primary

MeasureTime frame
Changes in the symptom-vaginal white discharge Foul smell vaginal itching vaginal burning sensation Burning Micturition Pain during intercourse Lower abdominal pain and any other associated symptomTimepoint: Baseline 15th 30th 45th 60th and 90th day

Secondary

MeasureTime frame
Changes in quality of life of the women in Swetapradara (Pathological leucorrhoea)Timepoint: Baseline 60th day and 90th day.

Countries

India

Contacts

Public ContactDR PRASHANT SHINDE

Regional Ayurveda Research Institute For Mother and Child Health Nagpur

dr.vanmala@gov.in9404669789

Outcome results

None listed

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