Platelet Rich Plasma for Uterine Scar
Recruiting now · Not applicable · Has a placebo group
Conditions studied: Cesarean Section Complications, Uterine Bleeding, Pelvic Pain, Menstrual Irregularity
In brief
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.
Key facts
- Study ID
- NCT05224726
- Run by
- The University of Texas Health Science Center, Houston
- People needed
- 40
- Starts
- 2025-07-19
- Expected to finish
- 2028-07-01
- Last updated by the study team
- 2025-08-26
Who can join
Age: 18 and older, up to 52. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Women undergoing elective cesarean delivery
- Term pregnancy (≥37 weeks of gestation)
You may not qualify if…
- Thrombocytopenia (CBC Platelet count <70,000)
- Connective tissue disease
- Uterine scars other than cesarean (s/p myomectomy, s/p cornual resection)
- Malformed uterus (unicornuate, bicornuate, didelphic)
Where it is running
- Sheba Medical Center — Ramat Gan, Center, Israel (enrolling)
Full record on ClinicalTrials.gov
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