A Comparative Clinical study to see the effect of some Ayurvedic formulation in patients of itching in vulva
Phase 2
- Conditions
- Health Condition 1: N768- Other specified inflammation of vagina and vulva
- Registration Number
- CTRI/2021/03/032120
- Lead Sponsor
- State Ayurvedic College and Hospital lucknow
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients willing to participate in trial
Adult Female who are in age group of 18-45 years
Only married patient
Patients having pruritus vulvae as a cardinal symptom with or without vaginal discharge
Exclusion Criteria
Patients below 18 years and above 45 years
Patients unwilling too participate in the trial Patients after menopause.
Patients who are willing to conceive.
Patients of uterine prolapse and Ca-cervix.
Patients on oral contraceptives or using intra uterine contraceptive device.
Patients with diabetes mellitus, tuberculosis,
severe hypertension, jaundice.
Patients with chronic cervicitis, fibroid and malignancy.
VDRL, HIV, HBsAg positive patient.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the efficacy of oral administration of Guduchidantyadi Vati and Guduchidantyadi Malahar in Pruritus vulvae <br/ ><br> <br/ ><br> <br/ ><br>Timepoint: Trial will be conducted for 1 month ( 21 days with medicine and 7 days without medicine) .Patient will be followed once a week during treatment and 7 days after the treatment is completed.
- Secondary Outcome Measures
Name Time Method To assess the efficacy of trial drug on subjective parameters white discharge p/v, malodor, vulvar pain , coital frequency , dyspareunia , burning micturition & inflammation in vulvaTimepoint: 1 month