Ovarian PRP (Platelet Rich Plasma) Injection for Follicular Activation

Last updated: May 29, 2025
Sponsor: University of Luebeck
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Infertility

Perimenopause

Treatment

autologous PRP (platelet rich plasma)

Saline solution (NaCL) Injection

Clinical Study ID

NCT05279560
Aktenzeichen 21-348
  • Ages 18-42
  • Female

Study Summary

The primary objective is to investigate the efficacy, defined as an increase in oocyte numbers upon ovarian stimulation, and safety of a single intra-ovarian PRP injection vs. saline solution (NaCl) injection (Placebo) transvaginally or laparoscopically for follicular activation in patients with child wish and with low ovarian reserve/expected poor ovarian response planning to undergo IVF or ICSI using own eggs. Pain score as numerical rating score and validated quality of life questionnaire will be requested after the procedure. Longterm follow-up of all participants will be performed 1, 2 and 5 years after end of study.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Serum AMH < 0.5 ng/ml (at screening visit and in the absence of OC or sex-steroidintake)

  • Antral follicular count (AFC) in both ovaries ≤ 5 (at screening visit and in theabsence of OC or sex-steroid intake)

  • Spontaneous cycle, menstrual cycle length 21-35 days

  • Body mass index (BMI) ≥18 kg/m2 and ≤38 kg/m2

  • Both ovaries must be visible by transvaginal ultrasound examination

  • Both ovaries must be judged accessible by transvaginal puncture

  • Indication for IVF or ICSI treatment

  • Willingness to participate and provide written consent prior to initiation of anystudy-related procedures

  • The subject and male partner must agree to participate in the infant follow-up ifshe becomes pregnant

  • The subject must be able to communicate well with the investigator and researchstaff and to comply with the requirements of the study protocol.

Exclusion

Exclusion Criteria:

  • ≥ four cumulus-oocyte-complexes (COCs) retrieved in a previous IVF cycles with aconventional stimulation protocol (within 6 months before enrollment)

  • Serum value of FSH ≥25 IU/l (within 12 months measured in the absence of OC orhormone replacement intake)

  • Thrombocytopenia defined as < 100.000 platelets/µl at screening

  • Oral contraceptive or sex steroid intake within 1 month prior to enrollment

  • Presence of structural or numerical chromosomal abnormality in cytogenetic analysis

  • Relevant autoimmune disease

  • History of malignancy and systemic chemotherapy or pelvic radiation

  • Severe endometriosis (stage III-IV)

  • Ovaries located outside the inner pelvis

  • Presence of unilateral or bilateral hydrosalpinx

  • Relevant endocrine disorders such as hypothalamic-pituitary disorder or thyroiddysfunction (except substituted Hashimoto's thyroiditis or latent hypothyroidism)

  • Relevant thrombophilic disorder

  • Contraindication for pregnancy

  • Contraindication for transvaginal ovarian puncture (such as previous major lowerabdominal surgery and known severe pelvic adhesion)

  • Uterine malformations or pathologies (such as sub mucosal fibroid(s), endometrialhyperplasia, endometrial fluid accumulation, or endometrial adhesions)

  • Mental disability or any other lack of fitness, in the investigator's opinion, topreclude subjects in or to complete the study

Study Design

Total Participants: 114
Treatment Group(s): 2
Primary Treatment: autologous PRP (platelet rich plasma)
Phase:
Study Start date:
March 17, 2022
Estimated Completion Date:
June 30, 2030

Study Description

Age-related infertility and premature loss of ovarian reserve has become a major challenge for ART professionals as the the average age at first child wish has dramatically increased over time. Under physiological circumstances, most follicles in the human ovary remain dormant throughout the female life span and eventually become atretic, however, histological samples reveal that the follicular pool in the ovary is completely exhausted only as late as the early 70ies and that the ovary holds oogonial stem cells, which may have the ability to differentiate into functional follicles. The pressing problem for reproductive medicine is therefore the question how to reactivate some of the putative ovarian 'reproductive reserve' in those women with premature follicular depletion or those who wish to become pregnant at advanced age.

Platelet rich plasma (PRP) is a blood-derived product, characterized by high concentrations of growth factors and chemokines. PRP is produced by centrifuging a small quantity of the patient's own blood and extracting the active, platelet-rich fraction. The platelet-rich fraction is applied to the human body typically by injection. PRP is used for therapeutic purposes in different medical areas ranging from orthopedics to plastic surgery, for its putative ability to stimulate and facilitate cell proliferation and thereby tissue differentiation and regeneration.

In the context of reproductive medicine, PRP has been proposed to increase pregnancy rates after uterine flushing in women with recurrent implantation failure or thin endometrium. Intra-ovarian injection of PRP has been proposed to activate dormant ovarian follicles pre IVF-treatment in cases of idiopathic low ovarian reserve, premature ovarian insufficiency or ovarian depletion because of advanced maternal age. To date, there is no randomized placebo-controlled trial available that has evaluated intra-ovarian PRP injection in terms of efficacy and safety for premature ovarian failure, and, more specifically, also not in patients with depleted ovarian reserve/poor ovarian response (POR) who constitute a significant proportion of patients undergoing assisted reproduction.

Connect with a study center

  • University of Luebeck

    Luebeck, Schleswig-Holstein 23562
    Germany

    Site Not Available

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