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NCT01868776 · ClinicalTrials.gov registry record · NA
Effect of Buffered Numbing Solution on Patients With Toothaches
A NA study of Irreversible Pulpitis (Toothache), sponsored by Ohio State University.
- Completed
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT01868776 is a NA study of Irreversible Pulpitis (Toothache) that has completed, run by Ohio State University. The registered enrollment target is 100 participants. The trial reports 1 study location across 1 state.
The verdict
NCT01868776, a NA study of Irreversible Pulpitis (Toothache), has completed, sponsored by Ohio State University.
- COMPLETED
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine the effect of buffered lidocaine (a numbing solution) on the ability to numb patients with toothaches. Buffered anesthetic (numbing) solutions have shown promise in some medical and dental research. Patients presenting with toothaches will be given either a buffered numbing solution or a nonbuffered numbing solution. Neither the patient nor the operator will know which solution they will receive. Root canal treatment will be performed on the tooth and the ability of the buffered versus non-buffered numbing solutions will be compared.
Conditions Studied
Interventions
- DRUG buffered lidocaine
- DRUG nonbuffered lidocaine
Study Locations (1)
Ohio
- The Ohio State University College of Dentistry, Postle Hall - Columbus
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2013-03 |
| Est. Completion | 2013-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01868776
The ClinicalTrials.gov registry entry for NCT01868776 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ohio State University, which has 552 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Irreversible Pulpitis (Toothache) appearing as the primary indexed condition, and to 2 interventions - of which buffered lidocaine is the first listed.
NCT01868776 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.
Frequently Asked Questions
What is clinical trial NCT01868776 about?
NCT01868776 is a clinical study titled "Effect of Buffered Numbing Solution on Patients With Toothaches". The purpose of this study is to determine the effect of buffered lidocaine (a numbing solution) on the ability to numb patients with toothaches. Buffered anesthetic (numbing) solutions have shown promise in some medical and dental research. Patients presenting with toothaches will be given either a ...
What is the current status of trial NCT01868776?
This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2013-03. Estimated completion is 2013-12.
What conditions does trial NCT01868776 study?
This clinical trial studies the following conditions: Irreversible Pulpitis (Toothache).
What interventions are being tested in trial NCT01868776?
The interventions under investigation include: buffered lidocaine (DRUG), nonbuffered lidocaine (DRUG).
Who is sponsoring clinical trial NCT01868776?
This trial is sponsored by Ohio State University, which has 552 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01868776 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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