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
This trial does not accept healthy volunteersQualifiers
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 population
Patients undergo endodontic emergency treatment.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Postoperative pain
Higher scores mean a worse outcome.
Secondary outcomes
Oral health-related quality of life
Higher scores mean a worse outcome.
Other outcomes
Prognostic factors associated with the improvement of postoperative pain
Prognostic factors associated with the improvement of oral health-related quality of life
Sponsors and contacts
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