IRCT20230722058884N1 IRCT 2023-11-30 Iran University of Medical Sciences Effect of Oral Furosemide on patients with preeclampsia during pregnancy Assessing the clinical effects of a short-term course of Oral Furosemide in postpartum period in patients with preeclampsia during pregnancy : A Randomized Controlled Trial 2023-09-23 anticipated 118 Complete https://irct.ir/trial/71611 interventional Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: The randomization protocol for this clinical trial is designed to ensure the unbiased allocation of participants into different treatment groups. Prior to the start of the trial, a computer-generated randomization list will be created by an independent statistician who is not involved in the recruitment or allocation process. Using this list, participants will be assigned to one of two treatment arms in a random manner. The randomization process will not be stratified The allocation sequence will be concealed from the researchers, participants, and study personnel until the intervention is assigned. This rigorous randomization process reduces the likelihood of selection bias, increases internal validity, and allows for a more accurate assessment of the treatment effects in the subsequent analysis, Blinding description: In this study only the patients will be blinded. 3 Unspecified pre-eclampsia. Intervention group: Patients with preeclampsia who are treated with ARB plus low does Furosemide. Undecided - It is not yet known if there will be a plan to make this available Justification or reason for indecision in sharing IPD is After publishing of the final data this will be discussed with the university's research council