Actively Recruiting
Risk of Nerve Damage After Administration of Local Anesthesia
Led by Cleveland Dental Institute · Updated on 2024-08-26
80
Participants Needed
2
Research Sites
65 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate of the risk of nerve damage following the administration of articaine 4% and lidocaine 2% for Inferior Alveolar nerve Block (IANB). A Randomized Controlled Clinical Trial will be conducted where the patient will be randomly assigned to one the two groups; articaine 4% and Lidocaine 2%. The type of LA will be concealed to the operator, investigators and assessors. The patients will be monitored for any aigns of nerve parathesia for 3 months after the procedure.
CONDITIONS
Official Title
Risk of Nerve Damage After Administration of Local Anesthesia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients between 18 and 55 years old
- Patients who need Inferior Alveolar Nerve Block (IANB)
- Healthy patients without significant medical conditions
You will not qualify if you...
- Presence of medical conditions
- Known allergies
- Current use of medications
- Pregnancy or breastfeeding
- Inability to provide informed consent
- Specific dental or medical history that may affect participation
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
Cleveland Dental Institute
Akron, Ohio, United States, 44703
Actively Recruiting
2
Cleveland Dental Institute
Ashtabula, Ohio, United States, 44004
Active, Not Recruiting
Research Team
P
Pablo R Velazquez, Resident
CONTACT
N
Nelson A Rendon, Resident
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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