Health Condition 1: N943- Premenstrual tension syndrome
Conditions
Interventions
None listed
Sponsors
Diksha Khathuria
Eligibility
Inclusion criteria
Inclusion criteria: Regular menstrual cycle of 21 35 days Women (married or unmarried) who are able to sign informed consent and demonstrate cooperative behaviour Fulfilling American College of Obstetrics Gynecology criteria for PMS Willing to participate and comply with treatment and follow up for the 2 month duration of the study
Exclusion criteria
Exclusion criteria: Irregular menstrual cycles Symptoms present for less than 2 cycles Participation in any clinical trial within 1 month Currently pregnant or breastfeeding History of mental disorders or ongoing psychiatric medication Known case of systemic disorders (e.g., hypothyroidism, heart disease, kidney disease, circulatory disorders, malignancy) Known drug allergies Diagnosed pelvic pathology on ultra-sonography
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in the signs and symptoms of Premenstrual Syndrome using the Daily Record of Severity of Problems (DRSP) Assessment Tool.Timepoint: 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Changes in the quality of life assessed using WHOQOLBREF Scale. (subset of 26 items taken from WHQOL-100) 2. Changes in inflammatory markers associated with PMS, such as CRP and ESR levels. Timepoint: 3 months | — |
Countries
India
Contacts
Public ContactAnu M S
Madan Mohan Malviya Govt. Ayurved College, Udaipur
Outcome results
None listed