A clinical study to evaluate the efficacy of oral administration of Nimbashatka choorna and Nimba malahara lepa with Vidangadi choorna and Nimba malahara lepa in itching per vagina.
Phase 2
- Conditions
- Health Condition 1: L292- Pruritus vulvae
- Registration Number
- CTRI/2024/07/071006
- Lead Sponsor
- Dr Gopika P
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)Subjects irrespective of marital status
2) Subjects in perimenopausal and post-menopausal age group
3)Subjects diagnosed with classical symptoms of Acharana yonivyapath
4)Subjects with classical symptoms of Pruritus vulvae.
5)Subjects willing to sign the consent form
Exclusion Criteria
1.Subjects who are pregnant and lactating mothers.
2.Subjects during the time of menstruation.
3.Subjects with uncontrolled diabetes mellitus.
4.Subject with known case of sexually transmitted diseases.
5.Subject with known case of benign and malignant conditions.
6.Subject with known case of systemic disorders.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method There is significant decrease in Pruritus vulvae which will be assessed based on 5-D Pruritus scaleTimepoint: Pre assessment 0th day <br/ ><br>1st assessment On 7th day <br/ ><br>Follow up On 15th day <br/ ><br>
- Secondary Outcome Measures
Name Time Method Generation of in-depth analysis of duration, degree, direction, disability & distribution of Pruritus vulvae <br/ ><br>Generation of data on possible unexpected drug reaction. <br/ ><br>Timepoint: 0th day to 15th day <br/ ><br>