Actively Recruiting
The Incidence of Postoperative Pain After Using Different Types of Sealers
Led by British University In Egypt · Updated on 2024-07-08
50
Participants Needed
1
Research Sites
113 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this randomized clinical trial is to evaluate and compare the incidence and intensity of post-operative pain after obturation using resin and silicon-based sealers.
CONDITIONS
Official Title
The Incidence of Postoperative Pain After Using Different Types of Sealers
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient's age ranges from 18-50 years old.
- Patients with teeth diagnosed with symptomatic irreversible pulpitis.
- Normal periapical condition confirmed by normal periapical radiograph.
- The teeth are restorable.
- Teeth are periodontally free, with no mobility and negative to percussion and palpation test.
You will not qualify if you...
- Teeth with immature roots.
- Non restorable teeth.
- Medically compromised patients with systemic complication that would alter the treatment.
- Necrotic teeth.
- Teeth with apical periodontitis or periapical lesions.
- Necrotic teeth.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
British University in Egypt
El Shorouk, Cairo Governorate, Egypt, +20 19283
Actively Recruiting
Research Team
K
Kareem Mohammed Elhoseny, ORCID:0009-0001-6101-5615, Bachelor
CONTACT
E
Engy Medhat Kataia, professor at BUE
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SCREENING
Number of Arms
2
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