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NCT02862691 · ClinicalTrials.gov registry record · Phase 2
Percocet vs. Bupivicaine for Toothaches in the ED
A Phase 2 study, sponsored by Stony Brook University.
- Terminated
- Registry status
- Phase 2
- Development phase
- 2
- Enrollment target
NCT02862691 is a Phase 2 study that was terminated before completion, run by Stony Brook University. The registered enrollment target is 2 participants.
The verdict
NCT02862691, a Phase 2 study, was terminated before completion, sponsored by Stony Brook University.
- TERMINATED
- Registry status
- Phase 2
- Development phase
- 2 participants
- Enrollment target
Study Summary
The goal of this study is to compare the speed and adequacy of pain relief in Emergency Department patients with a toothache after an oral analgesic or a local anesthetic administered as a nerve block or by local infiltration.
Interventions
- DRUG Acetaminophen/Oxycodone (Oral analgesic)
- DRUG Bupivicaine (Injectable local anesthetic)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2 participants |
| Start Date | 2016-08-01 |
| Est. Completion | 2017-08-01 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02862691
The ClinicalTrials.gov registry entry for NCT02862691 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 2 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Stony Brook University, which has 127 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Acetaminophen/Oxycodone (Oral analgesic) is the first listed.
NCT02862691 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02862691 about?
NCT02862691 is a clinical study titled "Percocet vs. Bupivicaine for Toothaches in the ED". The goal of this study is to compare the speed and adequacy of pain relief in Emergency Department patients with a toothache after an oral analgesic or a local anesthetic administered as a nerve block or by local infiltration.
What is the current status of trial NCT02862691?
This trial is currently terminated. It is a Phase 2 study. The enrollment target is 2 participants. The study started on 2016-08-01. Estimated completion is 2017-08-01.
What interventions are being tested in trial NCT02862691?
The interventions under investigation include: Acetaminophen/Oxycodone (Oral analgesic) (DRUG), Bupivicaine (Injectable local anesthetic) (DRUG).
Who is sponsoring clinical trial NCT02862691?
This trial is sponsored by Stony Brook University, which has 127 total clinical trials registered on ClinicalTrials.gov.
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