Trials / Completed
CompletedNCT01868776
Effect of Buffered Numbing Solution on Patients With Toothaches
Effect of Buffered Lidocaine on the Success of the Inferior Alveolar Nerve Block in Patients With Symptomatic Irreversible Pulpitis
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 100 (actual)
- Sponsor
- Ohio State University · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
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
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | buffered lidocaine | |
| DRUG | nonbuffered lidocaine |
Timeline
- Start date
- 2013-03-01
- Primary completion
- 2013-12-01
- Completion
- 2013-12-01
- First posted
- 2013-06-05
- Last updated
- 2020-10-06
- Results posted
- 2015-05-29
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01868776. Inclusion in this directory is not an endorsement.