Overview
A Comparison of IV Versus PO Acetaminophen Postoperatively for Opioid Consumption After Cesarean Section
Status:
Recruiting
Recruiting
Trial end date:
2020-06-23
2020-06-23
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
This randomized controlled study will compare narcotic consumption between two groups: patients that receive a perioperative dose of IV acetaminophen versus patients that receive a perioperative dose of oral liquid acetaminophen for scheduled cesarean section.Phase:
Phase 4Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Main Line HealthCollaborator:
Sharpe-Strumia Research FoundationTreatments:
Acetaminophen
Criteria
Inclusion Criteria:- Women age 18 or older
- Scheduled to undergo a cesarean section
Exclusion Criteria:
- Existing diagnosis of chronic pain
- Need to undergo a vertical skin incision
- Aspartate Aminotransferase (AST) > 50, alanine aminotransferase (ALT) > 70
- Platelets below 80,000 on admission
- Need to undergo general anesthesia
- Tubal ligation at time of Cesarean section
- Prior or known allergy to any of the medications being utilized in this study