Health Condition 1: N970- Female infertility associated withanovulation
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1 Patients of primary or secondary infertility due to anovulation or delayed ovulation 2 Patients having PCOD (Hyperandrogenic ovulatory dysfunction) 3 Irregular or scanty menses due to anovulatory cycle
Exclusion criteria
Exclusion criteria: ? Unmarried patients non-fertile age group patients ? Bleeding P/V ? Carcinoma of cervix, Vaginal polypoid growth ? Diagnosed patients of fibroids in uterus ? Inborn genital tract abnormality ? Endometritis due to tubercular infection ? HIV/VDRL/HbsAg positive ? Diagnosed subjects for malignancy ? Patients on hormonal treatment ? Non-Cooperative patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the ovulatory effects of trial drug To predict possible mode of action of trial drug on anovulatory menstrual cycle Timepoint: 120 days | — |
Secondary
| Measure | Time frame |
|---|---|
| To provide herbal cost effective better alternative in the management of anovulation in the patients of infertility To observe adverse drug reactions of trial drug if any during the trial & follow up period Timepoint: 120 days | — |
Countries
India
Contacts
MGACHRC, Salod, Wardha, Maharastra