Evaluation of heated anesthetic during anesthesia in childre
- Conditions
- ChildH02.163.876.600
- Registration Number
- RBR-4nh7hnt
- Lead Sponsor
- niversidade Federal de Santa Catarina
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Children between 7 and 10 years old are eligible; no systemic compromise; ASA I and II; both sexes; previous experience or not with dental anesthesia; need for dental treatment such as extractions, restorations and endodontic treatment in deciduous lower molars
Patients with acute pain; presence of odontogenic infection; emergency cases; history of bleeding or blood clotting problems; history of allergy to the drugs used in the research; history of asthma; liver disease; neurological disorders; use of analgesic or anti-inflammatory medication up to 5 hours before the procedure
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome assessed will be the report of pain during anesthetic injection, with the anesthetic solution heated to body temperature (37 °C) compared to anesthetic injection with a solution at room temperature (21 °C), both using 2% lidocaine 1: 100,000 with epinephrine, by measuring pain at the time of anesthetic injection. The instrument used to measure pain will be the Face, Legs, Activity, Cry, Consolability (FLACC) scale applied by a calibrated evaluator blinded to the anesthetic temperature. The application of the FLACC scale is done by observation, without the need for the child to respond, the patterns of face, legs, activity, crying and comfortability are evaluated, assigning scores from 0 to 3 for each item, with 0 = no pain and 3 = a lot of pain. This instrument will be applied during the infiltrative anesthesia procedure for lower primary molars.
- Secondary Outcome Measures
Name Time Method