Condition: Cesarean Delivery · Postpartum Hemorrhage (PPH) · Intraoperative Blood Loss · Sponsor: Wolfson Medical Center
The goal of this clinical trial is to learn whether applying topical tranexamic acid (TXA) directly to the uterine incision during cesarean delivery can reduce surgical bleeding compared to placebo. The study will include pregnant women aged 18-51 undergoing elective cesarean delivery at term (37 weeks or more). The main questions it aims to answer are: * Does topical TXA shorten uterine closure time? * Does topical TXA reduce the need for additional hemostatic sutures? Researchers will compare women receiving topical TXA to those receiving placebo (normal saline) to see if TXA reduces intraoperative bleeding and improves surgical outcomes. Participants will: * Be randomly assigned to receive either topical TXA or placebo during cesarean delivery. * Have standard surgery and postoperative care identical in both groups. * Provide routine clinical data, including hemoglobin levels and recovery outcomes, from their medical records.
This description comes directly from the study's public registry record.
Liat Mor · +972546738294 · liatmor1@gmail.com
Always discuss trial participation with your own doctor first.
| Edith Wolfson Medical Center | Holon, Central District, Israel | Recruiting |
| Meir medical center | Kfar Saba, Israel | Not Yet Recruiting |
| Rabin medical center | Petah Tikva, Israel | Not Yet Recruiting |
| Kaplan medical center | Rehovot, Israel | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT07362992