CTRI/2024/04/066481Not yet recruitingPhase 2
A randomized double blind comparative clinical trial to evaluate the efficacy of Vacha ( acorus calamus linn.) churna versus Shunthi (zingiber officinale roscoe.) churna in severe grade Premenstrual Syndrome - PMS- Premenstrual Syndrome
Shri Dhanwantry Ayurvedic College and Hospital Sector 46 B Chandigarh0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 2
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •Regular menstrual cycle of 21-35 days,Unmarried women age between 18-25years
- •Able to sign consent form and cooperative behavior
- •Severe grade PMS And PMDD Criteria (as per ICD 11 and DSM-V)
- •Symptoms Exist More Than 2 Cycles
Exclusion Criteria
- •Irregular cycle
- •Symptoms exists less than 2 cycles
- •History of any drug addiction
- •Patients participating in any other clinical trial 1 month back
- •Currently breastfeeding, pregnant
- •Ovariectomy, abortion, contraceptive usage within 6 months
- •Any history of mental disorder or patient on medication for that
- •Any systemic disorder like hypothyroidism , heart disease, kidney disease , circulatory system disease, malignant disease
- •Any history of allergic to any drug Pelvic pathology diagnosed with USG if any
Investigators
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