Patient Reported Outcomes and Associated Factors Following Endodontic Emergency Treatment

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorChulalongkorn University

About this trial

This study aims to analyze the improvement of postoperative pain and Oral Health-Related Quality of Life (OHRQoL) following endodontic emergency treatment, as well as the contributing factors affecting the change including age, gender, tooth type, dental arch, pulpal status, percussion pain, radiographic evidence of periapical lesions, type of emergency treatment (pulpotomy / partial pulpectomy / complete pulpectomy), and occlusal adjustment.

Eligibility criteria

Qualifiers

Age 18 years or older

Presence of moderate to severe pain as measured by a Numerical Rating Scale (NRS) score ≥ 4

Pain of endodontic origin confirmed through clinical and/or radiographic examination

Disqualifiers

Refused or were unable to provide informed consent or complete the questionnaire

Were currently or recently taking immunosuppressive agents, long-term anti-inflammatory medications, or antibiotics

Had non-endodontic or mixed-origin pain

Had already initiated endodontic treatment on the affected tooth

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Sponsors and collaborators