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Anesthetic Efficacy of Liposomal Prilocaine in Maxillary Infiltration Anesthesia

Phase 1
Completed
Conditions
Dental Anesthesia Efficacy
Interventions
Registration Number
NCT01073371
Lead Sponsor
University of Campinas, Brazil
Brief Summary

This blinded randomized, crossover, three period study aim to evaluate the anesthetic efficacy of liposome-encapsulated 3% prilocaine compared to 3% plain prilocaine and 3% prilocaine with 0,03IU/mL felypressin, after 1.8mL infiltration in the buccal sulcus of the maxillary right canine, in 32 volunteers.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
32
Inclusion Criteria
  • good health
  • no history of allergy to the components of the local anesthetic formulations tested
  • maxillary canine, lateral incisor, and first premolar responsible to electric stimulation
Exclusion Criteria
  • intake of any medication that would alter pain perception
  • history of trauma or sensitivity, caries, restorations, periodontal disease and endodontic treatment in the maxillary canine, lateral incisor, and first premolar
  • systemic disease

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
liposome-encapsulated 3% prilocainePrilocaine-
3% plain prilocainePrilocaine-
3% prilocaine with 0,03IU/mL felypressinPrilocaine-
Primary Outcome Measures
NameTimeMethod
Anesthesia success, onset and duration of pulpal and gingival anesthesia.10 minutes
Secondary Outcome Measures
NameTimeMethod
Injection pain - Visual Analogue Scale1 minute after the injections

Trial Locations

Locations (1)

Piracicaba Dental School

🇧🇷

Piracicaba, SP, Brazil

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