CompletedNot applicableNCT06978010
Efficacy of Platelet-rich Plasma in Improving Postoperative Scarring After Cesarean Delivery
Studying Rapidly involuting congenital hemangioma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Saint Andrew Hospital Constanta
- Principal Investigator
- Vlad Iustin Tica, ProffesorOvidius University
- Intervention
- Platelet-Rich Plasma (PRP) intraoperatively(other)
- Enrollment
- 100 target
- Eligibility
- 18-45 years · FEMALE
- Timeline
- 2023 – 2024
Study locations (1)
- Saint Andrew Hospital, Constanța, Constanța County, Romania
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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