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CLINICAL EFFECT OF PUGAKHANDA AND AYUSH PVK GEL ON WHITE DISCHARGE

Phase 2
Conditions
Health Condition 1: N948- Other specified conditions associated with female genital organs and menstrual cycle
Registration Number
CTRI/2020/07/026626
Lead Sponsor
CENTRAL COUNCIL FOR RESEARCH IN AYURVEDIC SCIENCES
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
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

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.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
Changes in quality of life of the women in Swetapradara (Pathological leucorrhoea)Timepoint: Baseline 60th day and 90th day.
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