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Study identifier: NCT05224726 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Platelet Rich Plasma for Uterine Scar

Condition: Cesarean Section Complications · Uterine Bleeding · Pelvic Pain  ·  Sponsor: The University of Texas Health Science Center, Houston

PhaseNA
Planned participants40
Who can joinFemale, 18 Years to 52 Years
Healthy volunteersYes

About this study

When vessel wall injury occurs, platelets become activated, releasing more than 30 bioactive proteins, many of which have a fundamental role in hemostasis, inflammation and ultimate wound healing. Platelet-rich plasma (PRP), a modification of fibrin glue made from autologous blood, is being used to deliver growth factors in high concentration to sites requiring wound healing. PRP is obtained from a sample of patients' blood drawn at the time of treatment. As the rate of cesarean deliveries has been rising, long-term adverse sequelae due to uterine scar defects have been increasing. PRP might be a simple preventive treatment that potentially can reduce morbidity following cesarean deliveries.

This description comes directly from the study's public registry record.

Talk to the study team

Aya A Mohr-Sasson, M.D  ·  3462704682  ·  mohraya@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Sheba Medical CenterRamat Gan, Center, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT05224726