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NCT05227300 · ClinicalTrials.gov registry record · Phase 4
Buffered vs. Unbuffered Local Anesthesia in Mandibular Molars Diagnosed With Symptomatic Irreversible Pulpitis
A Phase 4 study, sponsored by Indiana University.
- Completed
- Registry status
- Phase 4
- Development phase
- 40
- Enrollment target
NCT05227300 is a Phase 4 study that has completed, run by Indiana University. The registered enrollment target is 40 participants.
The verdict
NCT05227300, a Phase 4 study, has completed, sponsored by Indiana University.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 40 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether one type of anesthetic (numbing medicine) will work better at numbing the nerve in a tooth than using a different type of anesthetic. A second purpose is to see if the time needed to numb the nerve in a tooth is different between the two anesthetics.
Interventions
- DRUG 2% lidocaine with 1:100,000 epinephrine
- DRUG Onset Sodium Bicarbonate Inj., 8.4%, USP Neutralizing Additive Solution
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2022-02-14 |
| Est. Completion | 2022-06-30 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05227300
The ClinicalTrials.gov registry entry for NCT05227300 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Indiana University, which has 890 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which 2% lidocaine with 1:100,000 epinephrine is the first listed.
NCT05227300 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT05227300 about?
NCT05227300 is a clinical study titled "Buffered vs. Unbuffered Local Anesthesia in Mandibular Molars Diagnosed With Symptomatic Irreversible Pulpitis". The purpose of this study is to determine whether one type of anesthetic (numbing medicine) will work better at numbing the nerve in a tooth than using a different type of anesthetic. A second purpose is to see if the time needed to numb the nerve in a tooth is different between the two anesthetics.
What is the current status of trial NCT05227300?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 40 participants. The study started on 2022-02-14. Estimated completion is 2022-06-30.
What interventions are being tested in trial NCT05227300?
The interventions under investigation include: 2% lidocaine with 1:100,000 epinephrine (DRUG), Onset Sodium Bicarbonate Inj., 8.4%, USP Neutralizing Additive Solution (DRUG).
Who is sponsoring clinical trial NCT05227300?
This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.
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