Health Condition 1: null- Clomiphene citrate resistant polycystic ovarian sydrome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1 All patients of polycystic ovarian syndrome resistant to clomiphene citrate i.e patients who had received 6 cycles of clomiphene citrate or a maximun dose of 150 mg of clomiphene citrate and failed to ovulate 2 Patient with normal tubal patency by HSG or by laparoscopy 3 Normal semen analysis of the partner according to WHO 2013 criteria
Exclusion criteria
Exclusion criteria: 1 Patients with endometriosis 2 patients with abnormal TSH and prolactin levels 3 Patients with known etiologies like congenital adrenal hyperplasia,cushings syndrome,androgenic ovarian syndrome 4 Patients with endometrial tuberculosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1 Harmonal profile that is changes in the levels of LH FSH Testosterone Estradiol and Anti Mullerian Hormone will be measured 2 Pre and post intervention ultrasonographic characteristics such as changes in the ovarian volume and antral follicular count will be measured Timepoint: 1 month, 2 months, 3 months post procedure | — |
Secondary
| Measure | Time frame |
|---|---|
| 1 Post drilling peri tubal and peri ovarian adhesion formation 2 Any other factors contributing to infertility 3 Pregnancy out comeTimepoint: 2 years | — |
Countries
India
Contacts
AIIMS,New Delhi