Clinical trial of Manjishtha Kwath in painful menstruatio
Phase 2
- Conditions
- Health Condition 1: N944- Primary dysmenorrhea
- Registration Number
- CTRI/2022/07/043732
- Lead Sponsor
- Dr Monika Annasaheb Kate
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)female patients of age group 13-19 years
2) Patients with Primary Dysmenorrhoea
3) Diagnosed patients of Udavartini Yoniyapad according to symptoms.
4) Unmarried Female Patients
Exclusion Criteria
1) Patients of Secondary dysmenorrhoea
2) Married Female Patients
3) Patients with K/H/O fibroid, endometriosis, adenomyosis 4) K/H/O congenital anamolies of pelvic reproductive organ
5) K/H/O Oligomenorrhoea, PCOS, puberty menorrhagia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. To reduce the severity and incidence of pain during the menses <br/ ><br>2. To assess the pain with the help of VAS-SCALE <br/ ><br>3. To improve quality of life <br/ ><br>4. To reduce the incidence and severity of pain <br/ ><br>5. To study in detail the nidana, samprapti of udavartini yonivyapad and etiopathogenesis of primary dysmenorrhea <br/ ><br>6. To assess the improvement in the udavartini yonivyapad after treatment of 3 cyclesTimepoint: 3 months
- Secondary Outcome Measures
Name Time Method <br/ ><br>1. To reduce the severity and incidence of pain during the menses . <br/ ><br>2. VAS-SCALE <br/ ><br>3. To improve quality of life. <br/ ><br>4. Incidance and severity of pain can be reduced. <br/ ><br>5. To study in detail the nidana, samprapti of Udavartini Yonivyapad and etiopathogenesis of primary dysmenorrhoea <br/ ><br>6. To assess the improvement in the Udavartini Yonivyapad after treatment <br/ ><br>7. To achieve improvement in Udavartini Yonivyapad in a span of 4 months <br/ ><br>Timepoint: 3months