Autologous Platelet Rich Plasma Intraovarian Infusion for Poor Responders

Trial statusRecruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexFemale
Age35-47
SponsorGenesis Athens Clinic

About this trial

Autologous platelet rich plasma (PRP) intraovarian infusion may improve ovarian response to controlled ovarian stimulation as well as the hormonal profile of poor ovarian response infertile women subjected to intracytoplasmic sperm injection (ICSI) treatment.

Eligibility criteria

Qualifiers

Age ≥ 40 years

AMH < 1.1 ng/ml OR AFC < 7

≤ 3 oocytes with a conventional stimulation protocol

Discontinuation of any complementary/adjuvant treatment including hormone replacement and acupuncture, for at least three months prior to recruitment.

Disqualifiers

Any pathological disorder related to reproductive system anatomy

Cycle irregularities

Amenorrhea

Endometriosis

Trial design

Treatments tested in this trial

  • Autologous platelet rich plasma

Treatment groups

100 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Genesis Athens Clinic

Lead sponsor

National and Kapodistrian University of Athens

Collaborator