Skip to content

To investigate the effects of autologous platelet-rich plasma injection on ovarian parameters in patients with premature ovarian failure undergoing intracytoplasmic sperm injection

To investigate the effects of autologous platelet-rich plasma (PRP) injection on ovarian parameters in patients with premature ovarian failure (POF) undergoing intracytoplasmic sperm injection (ICSI)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250313065056N1
Enrollment
66
Registered
2025-09-15
Start date
2025-10-25
Completion date
Unknown
Last updated
2025-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Premature ovarian failure (POF). Primary ovarian failure

Interventions

Intervention 1: The intervention group received routine infertility treatment along with autologous platelet-rich plasma (PRP) injection. Blood was collected from each patient, and PRP was prepared un

Sponsors

Sanandaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: The study population included women aged 18–40 years who referred to the infertility centers of Besat Hospital and Dr. Masoumeh Rezaei Clinic during 2025–2026. They were diagnosed with premature ovarian failure (POF) based on laboratory and ultrasound findings, with AMH levels below 1. No male factor infertility was present, and all participants were in good general health.

Exclusion criteria

Exclusion criteria: Patients with platelet function disorders, hematologic diseases, or severe drug hypersensitivity were excluded from the study. Exclusion also applied to those with persistent use of nonsteroidal anti-inflammatory drugs (NSAIDs) within the last 48 hours Patients with active infection or febrile illness at the time of the study, and individuals taking medications that could interfere with treatment or test results. Patients with endocrine or metabolic disorders, as well as those diagnosed with polycystic ovary syndrome (PCOS)

Design outcomes

Primary

MeasureTime frame
Oocyte quality. Timepoint: Before the ovarian stimulation protocol and approximately 36 hours after HCG injection and follicular aspiration. Method of measurement: Oocyte quality was evaluated using a microscope after removal of granulosa cells.;Number of mature oocytes. Timepoint: Approximately 36 hours after HCG injection and follicular aspiration. Method of measurement: The number of mature oocytes was determined based on the Metaphase II stage.;Infertility treatment success rate. Timepoint: After intracytoplasmic sperm injection and follow-up of clinical outcomes. Method of measurement: Fertilization rates and pregnancy outcomes were recorded and followed up.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzra Allah Weisi

Sanandaj University of Medical Sciences

a.allahveisi@muk.ac.ir+98 87 3366 4645

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026