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Efficacy of Oral vs. Intravenous Acetaminophen

Primary Purpose

Postoperative Pain

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Oral Acetaminophen
Intravenous acetaminophen
Sponsored by
University of Texas Southwestern Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Postoperative Pain focused on measuring Acetaminophen, Postoperative pain, Sinus Surgery

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult patients aged 18 years or older
  • Undergoing elective sinus surgery at Zale Lipshy Hospital

Exclusion Criteria:

  • Inability of the patient to follow directions or comprehend either English or Spanish language.

    • Disorders of the liver which would make acetaminophen contraindicated (such as hepatitis, liver failure, prior liver transplant, etc).
    • Patients with chronic pain manifest by a baseline pain score > 4/10
    • Chronic opioid use (>2 weeks continuously), or illicit drug abuse
    • Body weight < 50 kg.
    • Patients with contraindications to any of the study drugs (such as Malignant Hyperthermia susceptible, celecoxib or sulfa allergy, etc.).
    • Patients who have taken analgesic medications on the morning of surgery (prior to arrival).
    • Allergy to acetaminophen

Sites / Locations

  • Zale Lipshy University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Oral Acetaminophen

Intravenous Acetaminophen

Arm Description

Oral Acetaminophen 1-hour before surgery

Intravenous Acetaminophen within 1-hour prior to anesthetic emergence

Outcomes

Primary Outcome Measures

Postoperative Pain Score on the Scale of 10 (0=No Pain and 10=Worst Pain)
Pain score on the scale of 10 at 1-h postoperatively in the Post-Anesthesia Care Unit (PACU)

Secondary Outcome Measures

Morphine Equivalents of Postoperative Opioid Usage
Total amount of postoperative opioid usage at Postoperative Anesthesia Care Unit (PACU), an expected average of 6 hours

Full Information

First Posted
June 2, 2015
Last Updated
April 20, 2020
Sponsor
University of Texas Southwestern Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02643394
Brief Title
Efficacy of Oral vs. Intravenous Acetaminophen
Official Title
The Comparative Efficacy of Oral vs. Intravenous Acetaminophen in Sinus Surgery Patients
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
August 17, 2015 (Actual)
Primary Completion Date
September 2, 2016 (Actual)
Study Completion Date
January 15, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Texas Southwestern Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The comparative efficacy of intravenous (IV) to oral (PO-'per os') acetaminophen in the management of postoperative pain is understudied and largely unknown. In this observer blinded randomized clinical trial, investigators aim to determine the comparative efficacy of PO (preoperative) vs. IV (intraoperative) acetaminophen in a sinus surgery population.
Detailed Description
The comparative efficacy of intravenous (IV) to oral (PO-'per os') acetaminophen is understudied and largely unknown. Intravenous acetaminophen has been available since 2010 (http://www.accessdata.fda.gov/drugsatfda_docs/label/2010/022450lbl.pdf) and has proven superiority over placebo in human clinical trials. It is clearly advantageous in patients who cannot take oral medications. Similarly, oral acetaminophen has proven efficacy in the management of postoperative pain. However, in patients who can receive either formulation the incremental cost of the IV formulation, both to the Health System and patient, is substantial. This incremental cost would be justifiable if there were clear efficacy or safety data to support the preferential use of IV over PO acetaminophen. However, there is no evidence of superior safety and there are only two studies to our knowledge investigating the question of comparative efficacy. Fenlon et al. randomized 130 patients undergoing 3rd molar (i.e., wisdom tooth) removal to IV vs. PO acetaminophen and found that PO acetaminophen was non-inferior to IV acetaminophen. The primary endpoint was postoperative pain score 1h after surgery. No safety concerns were identified in either group. Pettersson et al. randomized cardiac surgery patients to IV or PO acetaminophen, starting immediately postoperatively through the following morning, and found a significant opioid sparing effect of IV acetaminophen but no difference in pain scores or nausea. IV acetaminophen avoids first-pass hepatic metabolism and therefore generates higher serum and cerebrospinal fluid (CSF)/brain levels than does PO acetaminophen (http://ofirmev.com/Pharmacokinetics/). Based on the pharmacokinetic data, one can hypothesize that IV acetaminophen would be superior to PO acetaminophen at time points where serum and/or cerebrospinal fluid drug levels are higher.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Pain
Keywords
Acetaminophen, Postoperative pain, Sinus Surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
110 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Oral Acetaminophen
Arm Type
Active Comparator
Arm Description
Oral Acetaminophen 1-hour before surgery
Arm Title
Intravenous Acetaminophen
Arm Type
Active Comparator
Arm Description
Intravenous Acetaminophen within 1-hour prior to anesthetic emergence
Intervention Type
Drug
Intervention Name(s)
Oral Acetaminophen
Other Intervention Name(s)
Tylenol
Intervention Description
1000mg oral acetaminophen + 400mg oral celecoxib given within one hour of incision
Intervention Type
Drug
Intervention Name(s)
Intravenous acetaminophen
Other Intervention Name(s)
Tylenol
Intervention Description
400mg oral celecoxib given within one hour of incision + 1000mg IV acetaminophen within one hour prior to anesthetic emergence.
Primary Outcome Measure Information:
Title
Postoperative Pain Score on the Scale of 10 (0=No Pain and 10=Worst Pain)
Description
Pain score on the scale of 10 at 1-h postoperatively in the Post-Anesthesia Care Unit (PACU)
Time Frame
1-h postoperatively
Secondary Outcome Measure Information:
Title
Morphine Equivalents of Postoperative Opioid Usage
Description
Total amount of postoperative opioid usage at Postoperative Anesthesia Care Unit (PACU), an expected average of 6 hours
Time Frame
an expected average of 6 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients aged 18 years or older Undergoing elective sinus surgery at Zale Lipshy Hospital Exclusion Criteria: Inability of the patient to follow directions or comprehend either English or Spanish language. Disorders of the liver which would make acetaminophen contraindicated (such as hepatitis, liver failure, prior liver transplant, etc). Patients with chronic pain manifest by a baseline pain score > 4/10 Chronic opioid use (>2 weeks continuously), or illicit drug abuse Body weight < 50 kg. Patients with contraindications to any of the study drugs (such as Malignant Hyperthermia susceptible, celecoxib or sulfa allergy, etc.). Patients who have taken analgesic medications on the morning of surgery (prior to arrival). Allergy to acetaminophen
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David McDonagh, MD
Organizational Affiliation
UT Southwestern Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Zale Lipshy University Hospital
City
Dallas
State/Province
Texas
ZIP/Postal Code
75390
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Efficacy of Oral vs. Intravenous Acetaminophen

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