Clinical study for the evaluation of different local anesthetic dental techniques
- Conditions
- PeriodontitisDental AnxietyF01.470.132.300E03.155.141Anesthesia, Dental.C07.465.714.533
- Registration Number
- RBR-89rd4p
- Lead Sponsor
- niversidade Estadual de Ponta Grossa
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Patients should be at least 18 years of age with chronic periodontal disease, presenting at least one vital tooth with a clinical depth of probing greater than or equal to 4 mm in at least one of the probed sites in three different hemiarcates.
Patients in periodontal maintenance; sensitivity or any form of allergic reaction to amide-based anesthetics; have used analgesic or anesthetic medication for at least 12 hours prior to the periodontal instrumentation procedure; patients with previous history of alcoholism; pregnant or lactating women; patients with severe uncontrolled systemic disease such as heart, neurological, renal, hepatic or blood problems; psychiatric problems that could interfere with the scaling and smoothing or administration of topical anesthetics and injectables. Local pathological changes such as presence of ulcerative lesions, abscesses, acute infections; need for exodontia in the study quadrant; dentin hypersensitivity; absence of vitality or other pulp pathologies that could interfere in the measurement of the data in the teeth involved in the research.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method