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NCT01963754Phase 4
Key facts
Phase 4, randomised, double-blind trial of articaine (2 arms), sponsored by Implantology Institute. Primary endpoint: Anesthesia efficiency. Status: unknown.
Subepriosteal Articaine
Subperiosteal injection of Articaine 4% with 1:100,000 epinephrine.
Loco-regional Articaine
Loco-regional injection of Articaine 4% with 1:100,000 epinephrine.
Patients requiring single unit implant rehabilitation in the posterior mandible with at least 6mm residual bone and keratinized tissue. Excludes smokers, drug addiction, local anesthetic allergy, hepatic disease, immunodepression, pregnancy, diabetes, and heart disease.
Anesthesia efficiency
Intraoperatory Pain
Intraoperatory Anesthesia Complications
Post-Operatory Outcome Changes
Time of Surgery
Distance To Inferior Alveolar Nerve
Beyond the preview
Full results, competitive context and analysis are in the Gosset platform.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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