This randomized controlled trial is conducted on pediatric dental patients to compare the effectiveness of local anesthesia administered using a dental anesthesia injector device versus the traditional syringe method. The study aims to assess and compare pain and anxiety levels associated with both methods, using both subjective (self-reported) and objective measures. The goal is to identify an alternative technique that minimizes pain and anxiety in pediatric dental patients.
normal healthy patients (ASA I)
Undergoing the first dental local anesthesia experience
Presence of one at least vital deeply carious maxillary primary molar indicated for pulpotomy on each side of maxilla
Score 3 or 4 of Frankl scale of child behavior
Presence of gingivitis, dental abscess, facial trauma/ injury
Administration of analgesic 48 h before randomization
Presence of allergy from local anesthesia