None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: patients willing for trial and ready to give written consent married females in the age group between 20-45 yrs patients having clinical signs and symptoms of pathological leucorrhea abstinence from sexual intercourse during study period of minnimum of 2-4 weeks
Exclusion criteria
Exclusion criteria: patients not willing for the trial unmarried females pregnant females patients having unexplained vaginal bleeding history of use of antibiotics or local vaginal formulation taken within last 15 days patients suffering from uterine or cervical tumour, fibromyoma,polyp,prolapse or ovarian cyst patients having any systemic disorder like severe anaemia,DM,tuberculosis patients having endocervical smear positive for gonococci or positive VDRLor HIV test patients having abnormal pap smear with intraepithelial lesion or invasive cancer
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Relief in sign and symptoms of shweta pradara with Kush Moola Churna and Nyagrodh Twak Kashaya oral and local application respectively kin patientTimepoint: Relief in sign and symptoms of shweta pradara with Kush Moola Churna and Nyagrodh Twak Kashaya oral and local application respectively kin patient | — |
Secondary
| Measure | Time frame |
|---|---|
| To study cytological changes in Pap Smear. To study vaginal wet mount smear . To check the anti-microbial effect of Kush (Desmostachya bipinnata (Linn.) and Nyagrodh (Ficus Religiosa ( (Linn.) on culture. Timepoint: 3 months | — |
Countries
India
Contacts
RGGPG ayurvedic college and hospital paprola