Patient Reported Outcomes and Associated Factors Following Endodontic Emergency Treatment

Recruiting now

Conditions studied: Moderate to Severe Endodontic Pain

In brief

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.

Key facts

Study ID

NCT07192146

Run by

Chulalongkorn University

People needed

70

Starts

2023-08-17

Expected to finish

2025-10-01

Last updated by the study team

2025-09-25

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• Faculty of Dentistry, Chulalongkorn University — Bangkok, Thailand (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.