Studying the effect of Ajamodadi vati in women suffering from severe physical and mental symptoms preceding and during their menstruation.
Phase 3
- Conditions
- Health Condition 1: N943- Premenstrual tension syndrome
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Subjects fulfilling the diagnostic criteria.(Subjects should have at least 5 of the symptoms during the previous 2 consecutive cycles).
Age between 15-30 years.
Subjects with regular menstrual cycles.
Subjects willing to sign the written consent.
Exclusion Criteria
Known cases of pregnancy, breastfeeding, gynacological or psychological disorders.
Subjects on hormonal therapy or any medication that affects PMS symptoms.
Known cases of Congenital anomalies of the reproductive system.
Subjects having any systemic diseases likely to influence the menstrual cycle.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Determining the reduction of the physical symptoms of PMS in study group after intervention.Timepoint: Initiation of study - on day 1 <br/ ><br>1st follow up - after 2 weeks (on day 15) <br/ ><br>2nd follow up - after 4 weeks (on day 30) <br/ ><br>3rd follow up - after 8 weeks (on day 60) <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method Determining the improvement in quality of life in study group after intervention.Timepoint: Initiation of study - on day 1 <br/ ><br>1st follow up - after 2 weeks (on day 15) <br/ ><br>2nd follow up - after 4 weeks (on day 30) <br/ ><br>3rd follow up - after 8 weeks (on day 60)