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NCT02643394 · ClinicalTrials.gov registry record · Phase 4
Efficacy of Oral vs. Intravenous Acetaminophen
A Phase 4 study, sponsored by University of Texas Southwestern Medical Center.
- Completed
- Registry status
- Phase 4
- Development phase
- 110
- Enrollment target
NCT02643394 is a Phase 4 study that has completed, run by University of Texas Southwestern Medical Center. The registered enrollment target is 110 participants.
The verdict
NCT02643394, a Phase 4 study, has completed, sponsored by University of Texas Southwestern Medical Center.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 110 participants
- Enrollment target
Study 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.
Interventions
- DRUG Oral Acetaminophen
- DRUG Intravenous acetaminophen
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 110 participants |
| Start Date | 2015-08-17 |
| Est. Completion | 2018-01-15 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02643394
The ClinicalTrials.gov registry entry for NCT02643394 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 110 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Texas Southwestern Medical Center, which has 837 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Oral Acetaminophen is the first listed.
NCT02643394 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02643394 about?
NCT02643394 is a clinical study titled "Efficacy of Oral vs. Intravenous Acetaminophen". 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 (intra...
What is the current status of trial NCT02643394?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 110 participants. The study started on 2015-08-17. Estimated completion is 2018-01-15.
What interventions are being tested in trial NCT02643394?
The interventions under investigation include: Oral Acetaminophen (DRUG), Intravenous acetaminophen (DRUG).
Who is sponsoring clinical trial NCT02643394?
This trial is sponsored by University of Texas Southwestern Medical Center, which has 837 total clinical trials registered on ClinicalTrials.gov.
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