Pain After Buffered Vs Non Buffered Articaine
- Registration Number
- NCT06538233
- Lead Sponsor
- Cleveland Dental Institute
- Brief Summary
Pain after buffered versus non buffered articaine.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 108
Inclusion Criteria
- Males and females, age- 18 to 60 yrs.
- Medically free.
- Need a dental treatment in the upper anterior region.
Exclusion Criteria
- Periodontally affected teeth.
- Radiographic bone loss.
- Upnormal length of the teeth.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description non buffered articaine Non buffered articaine - Buffered articaine Buffered articaine -
- Primary Outcome Measures
Name Time Method Numerical Rate Scale (NRS) Immediate Pain during injection of buffered versus non-buffered articaine local anesthetic will be measured using NRS from 0 to 10, where 0 is no pain and 10 is the most unbearable pain .
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
How does buffering affect articaine's sodium channel blockade mechanism in pain management?
What is the comparative efficacy of buffered articaine vs lidocaine in dental anesthesia?
Which biomarkers correlate with reduced pain perception in buffered articaine trials?
What adverse events are reported with non-buffered articaine in phase 2 dental studies?
How do buffered amide local anesthetics like articaine compare to ester-based alternatives in pain control?
Trial Locations
- Locations (1)
Clevland Dental Institute
🇺🇸Cleveland, Ohio, United States
Clevland Dental Institute🇺🇸Cleveland, Ohio, United StatesPavanpreet Kaur, ResidentContact216-355-1155p.kaur@cdiohio.org