RCT (Randomized Controlled Trial) of IV Acetaminophen for Post Cesarean Pain Relief
Status:
Completed
Trial end date:
2017-05-01
Target enrollment:
Participant gender:
Summary
This study is being done to evaluate the scheduled use of intravenous (IV) acetaminophen
among cesarean section patients. The study hopes to find out if patients who receive
scheduled IV acetaminophen for 48 hours following delivery have lower self-reported pain
scores and use less narcotic pain medication than patients who do not receive IV
acetaminophen.