A clinical study to asses the effect of shunti in case of disease primary Dysmenorrhoea
Phase 3
- Conditions
- Health Condition 1: N944- Primary dysmenorrhea
- Registration Number
- CTRI/2023/04/051380
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Subjects suffering form kashtaartava having classical signs and symptoms.
subjects willing and able to participate in the study
Exclusion Criteria
Subjects who are not willing for the clinical study.
Subjects suffering from acute systemic disorders.
subjects who belong to pitta prakriti will be excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pain reduction <br/ ><br> <br/ ><br>Timepoint: 20days
- Secondary Outcome Measures
Name Time Method Reduction of pain during mensesTimepoint: 3 months