Status:
COMPLETED
Preoperative IV Versus Oral Acetaminophen
Lead Sponsor:
TriHealth Inc.
Conditions:
Pain, Postoperative
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
The current study proposes to examine whether there is a significant difference in patient outcomes related to the administration route of preoperative Acetaminophen. Specifically, the study will comp...
Detailed Description
This study will use a randomized, double-blind, controlled design with two arms: Arm 1: Scheduled IV Acetaminophen and PO placebo provided preoperatively Arm 2: Scheduled PO Acetaminophen and IV plac...
Eligibility Criteria
Inclusion
- 18 years old or older
- Admitted to Bethesda Butler Main Perioperative Services for an outpatient surgical procedure performed under general anesthesia
Exclusion
- Allergy to Acetaminophen
- Lactose intolerance or lactose allergy (placebo capsules contain lactose)
- Hepatic disease
- Having taken a product containing acetaminophen within 6 hours of scheduled surgery time
- Pregnant
- Weight less than 50kg
- Opioid addiction - admits to current opioid addiction and/or substance abuse disorder, and/or currently in treatment for opioid addiction or substance abuse
- Emergent or on-call procedures
- Inpatient surgery
Key Trial Info
Start Date :
April 1 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 12 2019
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT03468920
Start Date
April 1 2018
End Date
April 12 2019
Last Update
May 14 2019
Active Locations (1)
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1
TriHealth, Bethesda Butler Hospital
Cincinnati, Ohio, United States, 45011