Trial intelligence / Profile preview

Subperiosteal vs Loco-regional Articaine for Dental Implants

NCT01963754Phase 4

Key facts

Status
Unknown
Start
Apr 2017
Primary completion
Aug 2023
Countries
1
Sponsor
Implantology Institute
Modality
Small Molecules
01

Overview

Phase 4, randomised, double-blind trial of articaine (2 arms), sponsored by Implantology Institute. Primary endpoint: Anesthesia efficiency. Status: unknown.

02

Design

2 arms
Study design
RandomizedDouble-blind
  • 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.

03

Who it enrols

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.

04

Endpoints

Primary

  • Anesthesia efficiency

Secondary

  • Intraoperatory Pain

  • Intraoperatory Anesthesia Complications

  • Post-Operatory Outcome Changes

  • Time of Surgery

  • Distance To Inferior Alveolar Nerve

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