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Acetaminophen to Prevent Ischemic Oxidative Reperfusion Injury During Percutaneous Coronary Intervention for Acute Myocardial Infarction

Acetaminophen to Prevent Ischemic Oxidative Reperfusion Injury During Percutaneous Coronary Intervention for Acute Myocardial Infarction

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01120769
Acronym
APRIORI Pilot
Enrollment
0
Registered
2010-05-11
Start date
2011-07-31
Completion date
2012-07-31
Last updated
2015-12-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Myocardial Infarction

Keywords

Myocardial Infarction, Percutaneous Coronary Intervention, Acetaminophen, Lipid Peroxidation

Brief summary

The purpose of this study is to test the hypothesis that acetaminophen will reduce lipid peroxidation and isoprostane formation during reperfusion after percutaneous revascularization for acute myocardial infarction.

Interventions

DRUGAcetaminophen

single dose

DRUGPlacebo

single dose

Sponsors

Vanderbilt University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

\- Patients presenting with STEMI

Exclusion criteria

* Duration of symptoms \> 12 hours * Suspected LM or proximal LAD occlusion (based on EKG interpretation) * Hemodynamic instability * Acetaminophen use in prior 24 hours * Use of dipyridamole, or Aggrenox, a formulation of aspirin and extended-release dipyridamole, within 48 hours * Current use of the following medications: phenytoin, valproic acid, phenobarbital, topiramate, rifampin, carbamazepine, cyclophosphamide, ritonavir, efavirenz, St. John's Wort * Chronic heavy alcohol use * Chronic liver disease (other than non-alcoholic fatty liver infiltration) * Severe valvular heart disease * Stroke in the past 60 days * Active major bleeding * Major surgery in the past 30 days * Ongoing treatment for active malignancy * Life expectancy less than 12 months as determined by the patient's attending physician * Pregnancy * asthma or severe COPD * active wheezing on presentation * allergy or prior adverse reaction to adenosine

Design outcomes

Primary

MeasureTime frame
Plasma isoprostane level60 minutes

Secondary

MeasureTime frame
Index of microcirculatory resistanceAverage 20 minutes

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026