Actively Recruiting
Patient Reported Outcomes and Associated Factors Following Endodontic Emergency Treatment
Led by Chulalongkorn University · Updated on 2025-09-25
70
Participants Needed
1
Research Sites
110 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Patient Reported Outcomes and Associated Factors Following Endodontic Emergency Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Moderate to severe pain with a Numerical Rating Scale score of 4 or higher
- Pain confirmed to be of endodontic origin by clinical or radiographic exam
You will not qualify if you...
- Unable or unwilling to give informed consent or complete the questionnaire
- Currently or recently using immunosuppressive agents, long-term anti-inflammatory medications, or antibiotics
- Pain not caused by endodontic issues or of mixed origin
- Already started endodontic treatment on the affected tooth
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Faculty of Dentistry, Chulalongkorn University
Bangkok, Thailand, 10330
Actively Recruiting
Research Team
P
Pantira Thep-akrapong
CONTACT
C
Chanakarn Sinsareekul
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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