Analysis of different sealers used in root canal treatment on postoperative pain in endodontics.
- Conditions
- PulpitisC07.793
- Registration Number
- RBR-8s5cbfk
- Lead Sponsor
- niversidade Federal do Amazonas
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Men and women aged 18–65 years, diagnosed with symptomatic irreversible pulpitis with indication for endodontic treatment in permanent molar teeth, will be included in the study, confirmed by positive response to clinical, cold vitality and radiographic tests. The individual who participates in this research must have a contact number (phone or cell phone) to be able to carry out the post-operative evaluations.
Patients who were pregnant, immunocompromised, on medication or hypersensitive to anti-inflammatory drugs, or patients with occlusal disorders or any type of periodontitis or endodontic complications were excluded from the study, since these conditions would interfere with the analysis of the presence of pain after endodontic treatment.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the prevalence of postoperative pain after endodontic treatment in patients participating in the research in a period of 6, 12, 24, 48 and 72 hours and its intensity using a validated pain scale NRS type with a score of zero (no pain) up to 10 cm (maximum pain).
- Secondary Outcome Measures
Name Time Method The secondary outcomes will be worked with the statistical analysis of regression to verify if the occurrence of postoperative pain of the primary outcome could be being influenced by the possible accidental cases of overfilling or by the need of administration of rescue medication among the participants of the groups.