Trials / Terminated
TerminatedNCT02647892
Optimal Lidocaine Buffering to Reduce Injection Pain in Local Anesthesia
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 70 (actual)
- Sponsor
- University of Nebraska · Academic / Other
- Sex
- All
- Age
- 19 Years – 100 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine the optimal amount of lidocaine buffering needed to decrease injection pain when administering local anesthesia.
Detailed description
Once the site is chosen, the skin will be anesthetized as usual. This study will utilize a commercially prepared 1% lidocaine solution mixed with standard sodium bicarbonate. A total of 10 mL will be used.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | lidocaine | local anesthesia |
| DRUG | sodium bicarbonate | additional drug added to lidocaine |
Timeline
- Start date
- 2016-01-08
- Primary completion
- 2021-11-05
- Completion
- 2021-11-05
- First posted
- 2016-01-06
- Last updated
- 2023-08-21
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02647892. Inclusion in this directory is not an endorsement.