Postoperative pain and quality of life after Canal Treatment with mechanized instruments: clinical study
Not Applicable
- Conditions
- Pulp degenerationC07.793.237
- Registration Number
- RBR-10kbw6nx
- Lead Sponsor
- Centro Universitário do Maranhão - UNICEUMA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Ages between 18 and 50 years old; patients of both genders; diagnosed with pulp alteration with indication of radical endodontic treatment in molars; painless; no periapical lesion; with curvature of up to 25º and who sign the informed consent form
Exclusion Criteria
Presence of internal or external resorption; trismus; ankylosis; periodontal condition index less than 3; systemic disease; tooth positioning out of normal alignment; history of trauma; pregnancy; lack of patient compliance; and presence of teeth that require endodontic retreatment
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluate the painful response between the two systems over a period of 6, 12, 24 hours and daily for 3 days; using the visual scales method (NRS-10 cm and VAS-0-10 cm), based on the observation of a variation of at least 10% in pre- and post-intervention measurements
- Secondary Outcome Measures
Name Time Method It is expected to find an improvement in the patient's quality of life after endodontic treatment using the OHIP-14 scale method; based on the observation of a variation of at least 10% in pre- and post-intervention measurements