Status:
COMPLETED
Efficacy of IV Acetaminophen Versus Oral Acetaminophen
Lead Sponsor:
University of Rochester
Conditions:
Nephrectomy
Eligibility:
All Genders
18-89 years
Phase:
PHASE4
Brief Summary
The aim of this study is to determine whether intravenous acetaminophen compared to enteric acetaminophen offers increased efficacy in patients who are scheduled for laparoscopic donor nephrectomy and...
Eligibility Criteria
Inclusion
- Be at least 18 years old
- Be scheduled for donor nephrectomy or robot-assisted, laparoscopic nephrectomy for cancer at University of Rochester Medical Center
- Have cognitive ability to verbally rate their pain on the Numeric Rating Scale (NRS).
Exclusion
- Age younger than 18 years old or older than 90 years old
- Pregnancy (Pre-operative pregnancy test is standard of care for all elective operating room cases)
- Weight less than 50 kg
- Epidural use
- History of known liver disease.
- Patient unable to take enteral medications.
- Be taking opioid medications chronically.
Key Trial Info
Start Date :
August 8 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 10 2024
Estimated Enrollment :
214 Patients enrolled
Trial Details
Trial ID
NCT03365622
Start Date
August 8 2018
End Date
April 10 2024
Last Update
June 29 2025
Active Locations (1)
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1
University of Rochester Medical Center
Rochester, New York, United States, 14642