Randomized controlled clinical trial of patha churna vati in yoni kandu in kaphaj yonivyapad wsr candidiasis

Randomized controlled clinical trial of Patha churna vati in yoni kandu in kaphaj yonivyapad wsr candidiasis

Primary objective

To study the efficacy of patha churna vati in yoni kandu in kaphaj yonivyapad in comparison to fluconazole tablets

Secondary objective

To study yoni kandu wsr to candidiasis

To evaluate the efficacy of patha churna vati

Patients will be divided in two groups

Group A and Group B and will be given patha churna vati and fluconazole respectively for two weeks

Clinical assesment will be done on 1 st day 7th day 14th day and 21st day

Inclusion criteria is age 20 yrs to 40 yrs

Yoni kandu

Yoni strava

Yonigat toda

Exclusion criteria

Patients having excessive yoni toda

Pregnant women

Patients previously diagnosed with HIV HBSAG VDRL

Withdrawal criteria

The patient who wishes to discontinue and not ready for further participation in study will be discontinued

During the study if any complication occurs these patients will be excluded from the study and she will be given management accordingly

The patient who did not discontinued follow up for two consecutive visits will be treated as discontinued

Patients who are not ready to sign the written informed consent

Primary outcome

Reduce symptoms yoni kandu yoni strava yonigat toda

Secondary outcome

No recurrence of yoni kandu

All data will be collected from clinical case studies will be presented in the form of graphs charts healing grade

Patients will be observed before and after treatment

All observed data collected after the final assessment will be subjected to statistical analysis