Application of PRP-therapy in assisted reproductive technology
- Authors: Filimonova O.V.1, Pandya S.K.1, Osadchev V.B.1, Proklova G.F.1, Pobedinskaya O.S.1, Kanokova I.N.2, Safonova N.E.1
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Affiliations:
- Sechenov First Moscow State Medical University (Sechenov University)
- Sirius University of Science and Technology
- Issue: Vol 13, No 1 (2026)
- Pages: 25-33
- Section: Reviews
- Submitted: 26.01.2026
- Accepted: 20.03.2026
- Published: 31.03.2026
- URL: https://archivog.com/2313-8726/article/view/701863
- DOI: https://doi.org/10.17816/aog701863
- EDN: https://elibrary.ru/RPJRST
- ID: 701863
Cite item
Abstract
According to the World Health Organization, infertility affects 17.5% of the adult population worldwide and remains a serious medical and social challenge. Despite significant progress in assisted reproductive technologies, the treatment of infertility associated with endometrial disorder and ovarian dysfunction remains relevant and requires the search for new therapeutic approaches.
This review analyzes current data from Russian and international sources published over the past 5 years on the use of autologous platelet-rich plasma (PRP) as a promising therapeutic modality in assisted reproductive technology programs. The search for published data was conducted in PubMed, eLibrary, and Google Scholar databases. Analysis of the publications demonstrated that PRP therapy is clinically effective in treating thin endometrium, recurrent implantation failure, and premature ovarian insufficiency and may also improve the clinical pregnancy rate. However, the available studies are limited by small sample sizes and nonrandomized designs, precluding definitive conclusions regarding the efficacy and safety of PRP therapy. Additionally, different routes of administration, injected plasma volumes, and platelet concentrations are currently in use. However, their efficacy has not been compared against one another but only against control groups receiving conservative therapy. This technology requires further investigation in randomized clinical trials to develop standardized protocols and evaluate long-term outcomes.
Full Text
About the authors
Olga V. Filimonova
Sechenov First Moscow State Medical University (Sechenov University)
Author for correspondence.
Email: sfilimonova2014@gmail.com
ORCID iD: 0009-0002-4269-7320
Russian Federation, Moscow
Shati K. Pandya
Sechenov First Moscow State Medical University (Sechenov University)
Email: pandya_sh_k@student.sechenov.ru
ORCID iD: 0009-0006-8675-4066
SPIN-code: 8208-9227
Russian Federation, Moscow
Vasilii B. Osadchev
Sechenov First Moscow State Medical University (Sechenov University)
Email: osadchev_v_b@staff.sechenov.ru
ORCID iD: 0000-0001-5351-0854
SPIN-code: 1020-0592
MD, Cand. Sci. (Medicine), Associate Professor
Russian Federation, MoscowGuzel F. Proklova
Sechenov First Moscow State Medical University (Sechenov University)
Email: proklova_g_f@staff.sechenov.ru
ORCID iD: 0000-0003-3382-026X
SPIN-code: 3366-8200
MD, Cand. Sci. (Medicine)
Russian Federation, MoscowOlesya S. Pobedinskaya
Sechenov First Moscow State Medical University (Sechenov University)
Email: pobedinskaya-o@yandex.ru
ORCID iD: 0000-0002-1538-1219
SPIN-code: 6692-2199
MD, Cand. Sci. (Medicine)
Russian Federation, MoscowInna N. Kanokova
Sirius University of Science and Technology
Email: uterus1982@yandex.ru
ORCID iD: 0009-0004-1172-2540
MD, Cand. Sci. (Medicine)
Russian Federation, Federal Territory "Sirius"Natalia E. Safonova
Sechenov First Moscow State Medical University (Sechenov University)
Email: safonova_n_e@staff.sechenov.ru
ORCID iD: 0000-0002-9949-9192
SPIN-code: 3953-4695
MD, Cand. Sci. (Medicine)
Russian Federation, MoscowReferences
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