Ovarian Function Following Intraovarian Injection of PRP

Last updated: January 15, 2026
Sponsor: Center for Human Reproduction
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

N/A

Treatment

PRP - Platelet Rich Plasma

PPP - Platelet Poor Plasma

Clinical Study ID

NCT04278313
02102020-0
  • Ages 21-44
  • Female
  • Accepts Healthy Volunteers

Study Summary

Consenting women with evidence of poor ovarian reserve will be randomly assigned to treatment with either Platelet Rich Plasma (PRP) or Platelet Poor Plasma (PPP).

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • fewer than 6 oocytes in response to past ovulation induction

  • desire to establish a pregnancy using IVF

  • Age 44 years and under.

  • FSH > 12

  • AMH < 1.0

  • No Aspirin or Motrin for one week before treatment

Exclusion

Exclusion Criteria:

  • Age > 45 years

  • Marked thrombocytopenia

  • Blood diseases

  • Hypofibrinogenemia

  • Hemodynamic instability

  • Anticoagulant or antiaggregant treatment

  • Oncological diseases (specially, skeletal system and blood)

  • Sepsis

  • Acute and chronic infectious diseases

  • Autoimmune diseases, for example, lupus erythematosus, etc.

Study Design

Total Participants: 90
Treatment Group(s): 2
Primary Treatment: PRP - Platelet Rich Plasma
Phase:
Study Start date:
February 24, 2020
Estimated Completion Date:
December 31, 2026

Study Description

As women age oocytes are gradually depleted with a consequent progressive loss of ovarian function and fertility. When a woman's follicle cohort falls below a critical level, she enters a transitional time of diminished ovarian reserve known as ovarian aging. Recently the use of autologous platelet-rich plasma (A-PRP) has been proposed as an additional strategy for improving ovarian function. A-PRP is prepared from autologous blood using an FDA approved device. The rationale for the use of PRP is that it contains growth factors which stimulate cellular anabolism, inflammatory modulators that create an anti-inflammatory effect and fibrinogen which acts as a scaffold for regenerating tissue. The investigators hypothesize that the growth factors present in PRP may have a beneficial effect promoting growth and recruitment of antral follicles. The investigators will recruit a prospective cohort of 90 patients with evidence of Premature Ovarian Aging/DOR. Women invited to participate in this RCT will have FSH above 12 and AMH below 1.0 ng/mL respectively and will have had fewer than 6 oocytes retrieved in a previous ovulation attempt. Consenting participants in this trial will be randomized in a doubly blind fashion to two groups. One will receive Platelet Rich Plasma (PRP) and the other will receive Platelet Poor Plasma (PPP). Women assigned to PPP will be offerred PRP in a future cycle if they so desire.

Connect with a study center

  • Center for Human Reproduction

    New York, New York 10021
    United States

    Site Not Available

  • Center for Human Reproduction

    New York 5128581, New York 5128638 10021
    United States

    Site Not Available

Map preview placeholder

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.