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Patient Reported Outcomes and Associated Factors Following Endodontic Emergency Treatment

Patient Reported Outcomes and Associated Factors Following Endodontic Emergency Treatment: A Prospective Cohort Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07192146
Enrollment
70
Registered
2025-09-25
Start date
2023-08-17
Completion date
2025-10-31
Last updated
2025-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Moderate to Severe Endodontic Pain

Brief summary

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.

Interventions

None listed

Sponsors

Chulalongkorn University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Postoperative painFrom enrollment to the end of treatment at 2 yearsHigher scores mean a worse outcome.

Secondary

MeasureTime frameDescription
Oral health-related quality of lifeFrom enrollment to the end of treatment at 2 yearsHigher scores mean a worse outcome.

Other

MeasureTime frame
Prognostic factors associated with the improvement of postoperative painFrom enrollment to the end of treatment at 2 years
Prognostic factors associated with the improvement of oral health-related quality of lifeFrom enrollment to the end of treatment at 2 years

Countries

Thailand

Contacts

Primary ContactPantira Thep-akrapong
pantira.mew@gmail.com66813730370
Backup ContactChanakarn Sinsareekul
chanakarn.si@chula.ac.th66832759760

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026