An open label single arm clinical trial to evaluate the effect of Naarikela pushpaadi kashaya in Asrugdara (Dysfunctional Uterine Bleeding)
Phase 3
- Conditions
- Health Condition 1: N00-N99- Diseases of the genitourinary systemHealth Condition 2: N920- Excessive and frequent menstruation with regular cycleHealth Condition 3: N920- Excessive and frequent menstruation with regular cycle
- Registration Number
- CTRI/2021/02/031560
- Lead Sponsor
- SDM college of Ayurveda and hospital Hassan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Subject with menstral bleeding for more than 5 days in each cycle
Patient using more than 3 completely soaked pads per day
Intermenstrual bleeding
Subjects with signs and symptoms of Asrugdara for at least 3 months
Exclusion Criteria
Known case of threatened or incomplete abortion
Known case of coagulation and bleeding disorders
Known case of thyroid dysfunction
Known case of sexually transmitted diseases
Using intra Uterine and oral contraceptives
Known case of benign and malignant growth in uterus
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessment of symptoms such as excessive bleeding,prolonged bleeding,intermenstural bleeding,clotsAfter 2 months intervention (8 weeks) <br/ ><br>Assessment will be done.Timepoint: After 2 months intervention-1 month follow up
- Secondary Outcome Measures
Name Time Method Attainment of Regular menstruationTimepoint: 3months