Evaluation of the pain level of patients submitted to endodontic treatment with varying techniques, in order to identify the one that causes less pai
Not Applicable
Completed
- Conditions
- Caries with pulp exposureOral Health
- Registration Number
- ISRCTN16405594
- Lead Sponsor
- Pontifical Catholic University of Paraná
- Brief Summary
Results article in https://pubmed.ncbi.nlm.nih.gov/37431528/ (added 04/07/2024)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 170
Inclusion Criteria
1. Older than 18 years
2. Need endodontic treatment
3. Negative response to vitality tests
4. The included teeth were monoradicadic and biradicculated, superior and inferior, with or without image suggestive of periapical lesion
Exclusion Criteria
1. Acute apical pain and/or abscess
2. Endodontic retreatment
3. Pregnant women on antibiotics, corticosteroids or analgesics
4. Complications from systemic diseases
5. Anatomic diameter greater than the K-type file 20 mm or less than the K-type file 10, in addition to teeth with resorption and open apex
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain measured by a visual analogue scale, 6, 12, 24, 72 hours and 7 days after completion of treatment
- Secondary Outcome Measures
Name Time Method se of antidepressants and previous treatment of radiotherapy head and neck from patient records.