Infertility Clinical Trial
Official title:
Effect of Long, Short, and Ultrashort GnRH Agonist Treatment Protocols in Intracytoplasmic Sperm Injection Candidates on Ovarian Reserve
Verified date | December 2023 |
Source | Tanta University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study aimed to compare the gonadotropin-releasing hormone agonist (ultra-short) protocol versus (short and long) protocols on ovarian reserve in women undergoing intracytoplasmic sperm injection
Status | Completed |
Enrollment | 30 |
Est. completion date | December 1, 2023 |
Est. primary completion date | December 1, 2023 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 35 Years |
Eligibility | Inclusion Criteria: - women - aged between 18- and 35-years old - undergoing Intracytoplasmic sperm injection. Exclusion Criteria: - History of three or more previous In vitro fertilisation failures - Karyotypic abnormalities in either partner - Patients who previously undergo unilateral oophorectomy - Patients with chronic diseases (uncontrolled diabetes mellitus, cardiovascular diseases, liver and kidney failure) - Patients with diseases may affect In vitro fertilisation outcomes (Endometriosis, uterine fibroids, Hydrosalpinx, Adenomyosis, autoimmune diseases), polycystic ovary syndrome (PCOS) patients, poor responders (maternal age >40, Antral follicle counts (AFC)<5, Anti Mullerian Hormone (AMH)<1 and previous trial <5 oocyte retrieved) - Severe male factor, uterine abnormalities, adenomyosis and endometriosis - History of malignant tumors and related treatment, clinically significant systemic disease or abnormal hematology, chemistry, or urinalysis results at screening, non-ovarian causes (male or tubal factors with average ovarian reserve). |
Country | Name | City | State |
---|---|---|---|
Egypt | Ahmed M.E. Ossman | Tanta |
Lead Sponsor | Collaborator |
---|---|
Tanta University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Ongoing pregnancies | Number of ongoing pregnancies per woman randomized, defined as evidence of a gestational sac with fetal heart motion at 12 weeks or later, confirmed with ultrasound. | 12 weeks postintervention | |
Secondary | retrieved oocytes | Number of oocytes retrieved per woman randomized | 4 days postintervention | |
Secondary | Estradiol level | Estradiol level will be recorded | second day of menstruation | |
Secondary | Luteinizing Hormone level | Luteinizing Hormone level will be recorded | second day of menstruation | |
Secondary | Follicle-Stimulating Hormone level | Follicle-Stimulating Hormone level will be recorded | second day of menstruation |
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