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RCT (Randomized Controlled Trial) of IV Acetaminophen for Post Cesarean Pain Relief

Pain, Postoperative Clinical Trial

Official title:
Randomized Control Trial of IV Acetaminophen for Post Cesarean Delivery Pain Relief

Clinical Trial 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.

Clinical Trial Description

See Brief Summary ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02046382
Study type Interventional
Source TriHealth Inc.
Contact
Status Completed
Phase Phase 4
Start date January 2014
Completion date May 2017
View Details
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