Assessment of pain after adjustment occlusal in root canal treatment
- Conditions
- PulpitisK04.0
- Registration Number
- RBR-377483
- Lead Sponsor
- niversidade Federal do Amazonas (UFAM)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Healthy patients of both sexes (male and female) aged between 18 and 60 who have root canal treatment indication in molars permanent, diagnosed with irreversible pulpitis; presence of occlusal contact prior to endodontic treatment; presence of natural or artificial opposing tooth in the occlusal contact in treated endodontically teeth; to have phone number to contact.
Pregnant women, patients aged less than 18 and greater than 60 years, patients taking some anti-inflammatory medication or antibiotic treatment at the time, immunocompromised, with hypersensitivity to nonsteroidal anti-inflammatory; previous diagnosis of bruxism or clenching; absence of natural or artificial tooth opposite to the tooth to be treated endodontically; complications endodontic type: calcifications, external or internal resorption, partial formation of the apical apex with dental drilling, with longitudinal or vertical fractures and severe periodontal disease; treatments in multiple sessions; patients without phone contact.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Presence or absence of postoperative pain in endodontic treatment using WaveOne® system and performing occlusal adjustment, which will be checked by a scale measuring pain, verbal description, a reduction of 30% of the expected pain after treatment endodontic using only the Wave One® system and the results will be presented by percentages
- Secondary Outcome Measures
Name Time Method Will not be evaluated