patient with diminished ovarian reserve.
Conditions
Interventions
Intervention 1: In the intervention group, 1:35 cc of blood is taken from women. The blood sample is centrifuged at 1200 rpm for 12 minutes to separate the red blood cells. The extracted plasma is cen
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
No minimum to 42 Years
Inclusion criteria
Inclusion criteria: Women under the age of 42 Having a history of low ovarian reserve (less than 3 eggs in the previous IVF cycle) Abnormal laboratory tests anti mulerian hormone fewer than 1.1ng /dl Counting antral follicles 5-7 on transvaginal sonography
Exclusion criteria
Exclusion criteria: Women with anemia diagnosis history of malignancy Any endocrine disorders (hypothyroidism, hyperprolactinemia)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The rate of clinical pregnancy in the two groups undergoing PRGF and the PRP. Timepoint: 4 week after embryo transfer. Method of measurement: By seeing the fetal heartbeat on ultrasound. | — |
Secondary
| Measure | Time frame |
|---|---|
| The number of retrieved oocytes in the two groups injected with PRGF and PRP. Timepoint: During ovarian puncture. Method of measurement: counting. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZahra Razghandi
Shahid Beheshti University of Medical Sciences
Outcome results
None listed