92
Participants
Start Date
June 8, 2022
Primary Completion Date
November 30, 2023
Study Completion Date
November 30, 2023
Ketorolac
"Once the decision has been made by the primary obstetrics (OB) provider to proceed with cesarean delivery, participants will be randomized in to one of two groups:~* Single dose of intravenous (IV) Ketorolac 30mg Vs.~* Single dose of intravenous (IV) Ketorolac 60mg"
The Ohio State University Wexner Medical Center OB/GYN Maternal and Fetal Medicine, Columbus
Ohio State University
OTHER