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Recruiting Not applicable NCT07535190

Endometrial Immune Profile Changes After Autologous Intrauterine PRP Treatment

No applicable phase (e.g. observational)
Conditions: IVF Patients Female Infertility

Sponsor: Nadezhda Women's Health Hospital

trial.available_in: БГ
Overview
The success rate after treatment by in-vitro fertilisation (IVF) strongly depends on the endometrial receptivity, which in turn is strictly connected to the endometrial immune profile. IVF outcome is largely dependent upon endometrial immune cell ratios and their relationship with one another. During the last few years there are several studies and case reports for intrauterine PRP application in patients resulting in a thicker, regenerated endometrium and better immune cell population ratios. In this project, the investigators aim to analyze the effect of autologous intrauterine PRP administration on the endometrial immune profile, endometrial thickness, selected hormone levels (E2, P4) during the mid-luteal phase and IVF outcomes (biochemical and clinical pregnancy).
Who can participate
Inclusion Criteria: * Participating in Assisted Reproduction Treatment * Having infertility * Having regular menstrual cycles * Embryo transfer of euploid embryos Exclusion Criteria: * Uterine pathologies * Endometrial Bacterial infections * Active endometrial inflammation * Polycystic ovary syndrome * Cancer diagnostics * Positive HIV, HCV or HBV tests * Autoimmune diseases * Recent immune therapy
Interventions
Platelet rich plasma (PRP)
BIOLOGICAL
Locations 1
Bulgaria (1)
Nadezhda Women's Health Hospital
Sofia , Sofia
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Female only
Minimum age
18 Years
Maximum age
50 Years
Healthy volunteers
No
Start date
19.01.2026
Completion date
01.06.2028
Registry ID
NCT07535190
Source
clinicaltrials.gov
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