Risk of Nerve Damage After Administration of Local Anesthesia
Status unconfirmed · Phase 1
Conditions studied: Inferior Alveolar Nerve Injuries
In brief
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.
Key facts
- Study ID
- NCT06564987
- Run by
- Cleveland Dental Institute
- People needed
- 80
- Starts
- 2024-01-01
- Expected to finish
- 2025-03-31
- Last updated by the study team
- 2024-08-26
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Patients with age between 18-55 years old
- Patients need IANB
- healthy patient
You may not qualify if…
- medical conditions
- allergies
- medications
- pregnancy and breastfeeding
- inability to provide informed consent
- specific dental or medical history.
Where it is running
- Cleveland Dental Institute — Akron, Ohio, United States (enrolling)
- Cleveland Dental Institute — Ashtabula, Ohio, United States
Full record on ClinicalTrials.gov
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