A study to test the efficacy of Ayurvedic agents in the treatment of white discharge occurring during 2nd and 3rd trimester of pregnancy
Phase 1
- Conditions
- Health Condition 1: null- 2nd and 3rd trimester pregnent patients with white discharge per vagina
- Registration Number
- CTRI/2017/03/008175
- Lead Sponsor
- Institute for Post Graduation Teaching and Research in Ayurveda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age 20 to 40 years with different parity
2.2nd and 3rd Trimester of pregnancy
3.White discharge present during examination
4.Inflammation present in vulva and/or vagina
5.Micro-organisms present in vaginal discharge
Exclusion Criteria
1.1st Trimester of pregnancy
2.Age below 20 years or above 40 years with non-specific vulvovaginitis
2. Hypersensitivity to drug and inability to conform the protocol
3.Women with severe physical illness, any organic pathology, hepatic, cardiac, renal disease and any acute infection of any system
4.Women suffering from any systemic disease like Diabetes, T.B., S.T.Ds etc.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1Screening of the antenatal patients attending the OPD of SRPT Dept IPGT And RA to elicit etiopathogenesis and prevalence of the condition of Upapluta Yonivyapad vulvovaginitis during pregnancyTimepoint: 1 Screening of the antenatal patients attending the OPD of SRPT Dept IPGT and RA to elicit etiopathogenesis and prevalence of the condition of Upapluta Yonivyapad vulvovaginitis during pregnancy
- Secondary Outcome Measures
Name Time Method To assess and compare the efficacy of both drugs Dhatakyadi Varti and Panchavalkaladi Varti in the management of Upapluta Yonivyapad (vulvovaginitis during pregnancy).Timepoint: 14 days