Health Condition 1: N943- Premenstrual tension syndrome
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Married and unmarried females of age group 20 45 years Patients willing to participate in this trial through written informed consent Patients fulfilling the criteria of mild to moderate PMS as per PMSS
Exclusion criteria
Exclusion criteria: Females with menstrual irregularities Menstrual or gynecological disorders such as endometriosis, fibroid Allergy or hypersensitivity to treatment ingredients Use of hormonal contraceptives or treatments (birth control pills, hormone replacement therapy within last 3 months) Severe medical conditions such as Hyperthyroidism (TSH less than 0.1mIU/L), Anemia (Hb less than 7 gm/dl) Pregnant or lactating women Lactose intolerance (Because Trial drug Ashwagandha will be administered with milk)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in PMSS scoreTimepoint: 8 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Change in menstrual patternTimepoint: 8 weeks | — |
Countries
India
Contacts
National Institute of Ayurveda