Comparison of the effect of Laser protocol and Cryotherapy on the occurrence of postoperative pain in inflamed molar teeth
- Conditions
- Pulpitis
- Registration Number
- RBR-7xz8bvw
- Lead Sponsor
- niversidade Federal do Amazonas
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Capable adult patients; aged between 18 and 65 years; both genders; who already have an indication for endodontic treatment in permanent molar teeth; diagnosed with irreversible pulpitis, confirmed by a positive response to clinical, electrical sensitivity and radiographic tests; have a contact number (telephone or cell phone or username on social networks) to be able to carry out postoperative evaluations
Patients who are at any stage of pregnancy. Patients who have been taking any medication such as analgesics or anti-inflammatories in the last 48 hours or who are immunocompromised, as these factors may alter the perception of pain or interfere with the analysis of the post-treatment pain score. Patients who have teeth with endodontic complications, such as: calcifications, external or internal resorption, partial formation of the apex, with dental perforations, with longitudinal or vertical fractures or with severe periodontal disease. During the endodontic procedure, patients who cannot have the endodontic treatment completed in the same session, or those patients who for any reason cannot be contacted to perform the outcome assessment will be excluded.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the occurrence and intensity of post-operative endodontic pain by applying a discrete numeric scale marked from zero (no pain) to 10 cm (maximum pain), in patients participating in the research over a period of 6, 12, 24, 48 and 72 hours after endodontic treatment.
- Secondary Outcome Measures
Name Time Method It is expected to find a lower occurrence and intensity of postoperative pain in the intervention group, with a difference of 25% between the groups