Tranexamic acid in pregnant women with placenta previa: a double-blind, multicenter randomized clinical trial

HIGHLIGHTS

• What: Randomization and blinding A total of 149 participants were randomly assigned to two groups in a 1:1 ratio by a statistician at the College of Medicine, who was blinded to the research purposes, using a random allocation software program (version 2.0) . The individual responsible for data collection was blinded to the research purpose and the UI codes. The data were evaluated regularly to monitor participant outcomes, safety, and the impact of interventions, as well as to evaluate the performance in achieving the study objectives. The lack of data on maternal outcomes specific to placenta . . .
  

   

  

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