{"protocolSection":{"identificationModule":{"nctId":"NCT03209687","orgStudyIdInfo":{"id":"3778"},"briefTitle":"The Value of Addition of Human Menopausal Gonadotropin Drug Following Oocytes Retrieval in IVF Cycles","officialTitle":"Human Menopausal Gonadotropin as a Novel Addition to Luteal Phase Support in Down-regulated ICSI Cycles (RCT)"},"descriptionModule":{"briefSummary":"The aim of this study is to test the hypothesis that addition of daily small dose of human menopausal gonadotropin (HMG) drug following oocytes retrieval could improve the fertility outcome in women undergoing in-vitro fertilization","detailedDescription":"The study will be conducted in the IVF unit of Cairo University. Females undergoing ICSI cycles in the age between 20 and 40 years will be allocated to one of 2 groups. Long agonist protocol will be used. Allocation to either one of 2 groups will be done on the day of oocytes retrieval. The first group will take (in addition to the routine care) daily human menopausal gonadotropin drug injection for 2 weeks. The second group will receive the routine care."},"conditionsModule":{"conditions":["Infertility"]},"eligibilityModule":{"eligibilityCriteria":"Inclusion Criteria:\n\n* Females undergoing Intra-Cytoplasmic Sperm Injection (ICSI) cycles\n* Age between 20 and 40 years\n\nExclusion Criteria:\n\n* Females who have high response (estradiol at time of ovulation trigger is \\> 5000 pg/ml or more than 15 oocytes are retrieved)","healthyVolunteers":false,"sex":"FEMALE","minimumAge":"20 Years","maximumAge":"40 Years","stdAges":["ADULT"]}}}