Poor ovarian response. Female infertility associated with anovulation
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Age group 20-40 years POSEIDON poor responder group 3 and 4 (expected poor responder group with AFC <5 and antimüllerian hormone (AMH) less than 1.1 ng/ml) Ovulation induction by GnRH antagonist protocol Normal parameters of semen Sperm intracytoplasmic injection Willingness to participate in the study and provide written informed consent Injection of platelet-rich plasma into the ovary
Exclusion criteria
Exclusion criteria: Contraindications for intracytoplasmic sperm injection(ICSI) treatment Contraindications to the use of granulocyte colony-stimulating factor and dydrogesterone Inability to fully comply with the study protocol In the last 3 months, G-CSF has been used for treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| GDF9 gene expression level in granulosa cells in GCSF and normal saline treated groups. Timepoint: The measurement of GDF9 gene expression in granulosa cells is at the end of the study and after collecting the follicular fluid of the entire sample volume. Method of measurement: Polymerase Chain Reaction.;BMP15 gene expression level in granulosa cells in GCSF and normal saline treated groups. Timepoint: The measurement of BMP15 gene expression in granulosa cells is at the end of the study and after collecting the follicular fluid of the entire sample volume. Method of measurement: Polymerase Chain Reaction.;The level of FLT1 gene expression in granulosa cells in GCSF and normal saline treated groups. Timepoint: The measurement of FLT1 gene expression in granulosa cells is at the end of the study and after collecting the follicular fluid of the entire sample volume. Method of measurement: Polymerase Chain Reaction.;HIF1 gene expression level in granulosa cells in GCSF and normal saline treated groups. Timepoint: The measurement of HIF1 gene expression in granulosa cells is at the end of the study and after collecting the follicular fluid of the entire sample volume. Method of measurement: Polymerase Chain Reaction.;Number of mature oocyte. Timepoint: After collecting the oocytes. Method of measurement: Counting in the laboratory.;Follicular fluid AMH. Timepoint: At the end of the study and after collecting the follicular fluid of the total sample volume. Method of measurement: Using the kit.;Follicular fluid FSH. Timepoint: At the end of the study and after collecting the follicular fluid of the total sample volume. Method of measurement: Using the kit. | — |
Countries
Iran (Islamic Republic of)
Contacts
Shiraz University of Medical Sciences