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Clinical Trial Summary

This is a randomized control, double-blind study in which women who are about to go an elective vaginal hysterectomy are offered to participate. Patients will be randomly assigned to one of two groups: the tranexamic acid group, in which 1 gram of tranexamic acid (Hexakapron) is administered intravenously before surgery, and the control group, in which patients will receive 10 ml of normal saline 0.9% intravenously.


Clinical Trial Description

This is a randomized control, double-blind study in which women who are about to go for an elective vaginal hysterectomy are offered to participate. Patients will be randomly assigned to one of two groups: the tranexamic acid group, in which 1 gram of tranexamic acid (Hexakapron) is administered intravenously before surgery, and the control group, in which patients will receive 10 ml of normal saline 0.9% intravenously. A nurse will prepare the solution according to the randomization and will handle it to the anesthesiologist. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05921071
Study type Interventional
Source Wolfson Medical Center
Contact Ohad Gluck
Phone 0528702255
Email ohadgluck@gmail.com
Status Recruiting
Phase N/A
Start date January 22, 2023
Completion date January 1, 2025

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