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Clinical Trials/RBR-5g4p9q8
RBR-5g4p9q8
Recruiting
未知

Assessment of a cryotherapy protocol on the occurrence of postoperative endodontic pain in molars with irreversible pulpitis: a randomized clinical trial

niversidade Federal do Amazonas0 sitesApril 29, 2024

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
niversidade Federal do Amazonas
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 29, 2024
End Date
November 2, 2024
Last Updated
last year
Study Type
Intervention

Investigators

Sponsor
niversidade Federal do Amazonas

Eligibility Criteria

Inclusion Criteria

  • The inclusion criteria will involve recruiting capable adult patients (18 to 65 years old) who already have an indication for endodontic treatment in permanent molars, diagnosed with irreversible pulpitis confirmed by a positive response to clinical, electrical sensitivity, and radiographic tests. Individuals participating in this research must provide a contact number (phone, cell phone, or social media username) to facilitate postoperative assessments. If a patient requires endodontic treatment for more than one tooth, the operator will follow the standard protocol; however, such cases will not be included in the study to avoid selection bias in the sample.

Exclusion Criteria

  • Patients in any stage of pregnancy, those currently taking medication such as analgesics or anti\-inflammatories at the time of treatment, immunocompromised individuals, or those with hypersensitivity to non\-steroidal anti\-inflammatory drugs will not participate in the study. These factors may alter pain perception or interfere with the analysis of post\-treatment pain scores.
  • Patients with teeth presenting endodontic complications, such as calcifications, external or internal resorption, partial apex formation, dental perforations, longitudinal or vertical fractures, severe periodontal disease, or those undergoing treatment in multiple sessions, will also be ineligible for participation in this study. These factors can interfere with proper endodontic therapy and, consequently, with postoperative pain. Data from patients who cannot be contacted for postoperative pain assessment for any reason will be excluded.

Outcomes

Primary Outcomes

Not specified

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