Health Condition 1: E282- Polycystic ovarian syndrome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Female participants of age group 18-34 years Female participants diagnosed with PCOS according to Rotterdam’s criteria Participants who have consented for research participation
Exclusion criteria
Exclusion criteria: Participants having other morbidity which mimics PCOS, immune compromised patients, participants suffering from severe psychiatric disorder and participants having substance abuse Participants with History of Oral Contraceptive Pill use (4 weeks prior to enrollment) Participants who are Pregnant and lactating Participants on homoeopathic treatment previously
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes will be observed in PCOSQ scale Changes can be positive or negative or no changeTimepoint: PCOSQ scale will be used at baseline, at every month upto 24 weeks 15 months study 6 months enrolment 6 months follow up 3 months analysis First dose at the time of case taking and subsequent doses according to follow ups | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: Not Applicable | — |
Countries
India
Contacts
Bakson Homoeopathic Medical College and Hospital