Evaluation of the effect of PRP on the outcome of IVF cycle in poorly responding patients.
Conditions
Interventions
The present study is a before and after clinical trial study that will be conducted in Shahid Beheshti Hospital, Kashan. This study will be conducted on 15 poor responder patients of group 3 and 1 pos
Sponsors
Kashan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
No minimum to 35 Years
Inclusion criteria
Inclusion criteria: This study will be conducted on 15 poor responder patients of group 3 and 1 poseidon. Inclusion criteria: age less than 35 years, BMI less than 30 and AMH1.2 ng/ml AFC >5 (Group 1 of Poseidon).
Exclusion criteria
Exclusion criteria: Hematological disorders (leukemia, thrombocytopenia), immunological disorders (antiphospholipid syndrome, thrombophilia), hormonal disorders (diabetes, thyroid, hyperprolactinemia), chromosomal and genetic abnormalities (hereditary or congenital) and kidney failure.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Endometrial thickness. Timepoint: Before entering the cycle on the fifth day of the eighth and three months later. Method of measurement: Ultrasound.;Oocyte count. Timepoint: Before entering the cycle on the fifth day of the eighth and three months later. Method of measurement: Ultrasound (sonography). | — |
Secondary
| Measure | Time frame |
|---|---|
| ANTI MOULLERIAN HORMON. Timepoint: Before entering the cycle on the fifth day of the eighth and three months later. Method of measurement: Measurement by blood test analysis after eight hours of fasting and without intimacy and stress the night before.;Follicle-stimulating Hormone. Timepoint: Before entering the cycle on the fifth day of the eighth and three months later. Method of measurement: Measurement by blood test analysis after eight hours of fasting and without intimacy and stress the night before. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactzahra usefi
Kashan University of Medical Sciences
Outcome results
None listed