Overview

Effect of GnRH Agonist Treatment Protocols on Ovarian Reserve

Status:
Not yet recruiting
Trial end date:
2023-04-14
Target enrollment:
0
Participant gender:
Female
Summary
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
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Tanta University
Treatments:
Hormones
Criteria
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).