Buffered 2% articaine in buccal infiltration of mandibular molars: a randomized triple-blind clinical trial
Braz. oral res. (Online)
; 37: e132, 2023. tab, graf
Article
ي En
|
LILACS-Express
| LILACS, BBO
| ID: biblio-1528132
المكتبة المسؤولة:
BR1.1
ABSTRACT
Abstract This crossover study aimed to compare the anesthetic effects of buffered 2% articaine with 1200,000 epinephrine with that of non-buffered 4% articaine with 1200,000 epinephrine. Forty-seven volunteers were administered two doses of anesthesia in the buccal region of the second mandibular molars in two sessions using 1.8 mL of different local anesthetic solutions. The onset time and duration of pulp anesthesia, soft tissue pressure pain threshold, and the score of pain on puncture and burning during injection were evaluated. The operator, volunteers, and statistician were blinded. There were no significant differences in the parameters onset of soft tissue anesthesia (p = 0.80), duration of soft tissue anesthesia (p = 0.10), onset of pulpal anesthesia in the second (p = 0.28) and first molars (p = 0.45), duration of pulp anesthesia of the second (p = 0.60) and first molars (p = 0.30), pain during puncture (p = 0.82) and injection (p = 0.80). No significant adverse events were observed. Buffered 2% articaine with 1200,000 epinephrine did not differ from non-buffered 4% articaine with 1200,000 epinephrine considering anesthetic success, safety, onset, duration of anesthesia, and pain on injection.
النص الكامل:
1
الفهرس:
LILACS
نوع الدراسة:
Clinical_trials
اللغة:
En
مجلة:
Braz. oral res. (Online)
موضوع المجلة:
ODONTOLOGIA
السنة:
2023
نوع:
Article
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Project document