Oral Acetaminophen Use for Pain Reduction in Electrophysiology Procedures
Status unconfirmed · Phase 4 · Has a placebo group
Conditions studied: Post Electrophysiology Procedure Pain
In brief
The investigators are purposing a study to evaluate the use of acetaminophen given prior to an electrophysiology procedure and post procedural pain control.
Key facts
- Study ID
- NCT03702023
- Run by
- Ascension Health
- People needed
- 200
- Starts
- 2019-02-08
- Expected to finish
- 2020-06-01
- Last updated by the study team
- 2019-07-02
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age: Over 18
- Weight: Greater than 50kg
- Scheduled for an EP procedure
- Be able to take oral medications
- Provide signed written informed consent
You may not qualify if…
- Have chronic pain requiring the use of chronic pain medications including narcotic pain medications or chronic acetaminophen use greater than seven consecutive days prior to the procedure
- Known hypersensitivity to acetaminophen
- Known or suspected history of alcohol or drug abuse/dependence within the previous 2 years
- Known impaired liver function
- Active pregnancy
Where it is running
- Ascension Genesys Hospital — Grand Blanc, Michigan, United States
Full record on ClinicalTrials.gov
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