Actively Recruiting
The Effect of Different Obturation Techniques on Postobturation Pain in Single-Visit Root Canal Treatment
Led by Kafrelsheikh University · Updated on 2024-06-06
150
Participants Needed
1
Research Sites
30 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this prospective clinical randomized study is to evaluate the effect of different obturation techniques on postobturation pain in single-visit root canal treatment in 18-60 years old patient who present no systemic disease (American Society of Anesthesiology class I or II) and require nonsurgical root canal treatment The main question it aims to answer which obturation technique used with bioceramic sealer cause less postobturation pain in single-visit root canal treatment in comparison to AH plus sealer used with lateral condensation or warm vertical compaction. Participants will receive single visit root canal treatment using bioceramic sealer with different obturation techniques Group 1: Single cone technique Group 2: lateral condensation technique Group 3: Vertical compaction technique to see effect of different obturation technique on postobturation pain in single-visit root canal treatment.
CONDITIONS
Official Title
The Effect of Different Obturation Techniques on Postobturation Pain in Single-Visit Root Canal Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18-60 years with no systemic disease (American Society of Anesthesiology class I or II) requiring nonsurgical root canal treatment
- Diagnosis of asymptomatic irreversible pulpitis in a molar tooth with 3 independent root canals
You will not qualify if you...
- Presence of immature root apexes, root fracture, or periodontal disease
- Use of any analgesic, anti-inflammatory, or antibiotics before the treatment
AI-Screening
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Trial Site Locations
Total: 1 location
1
kafrelsheikh University
Kafr ash Shaykh, Kafr El-Shaikh, Egypt, 33511
Actively Recruiting
Research Team
H
Hisham Abada, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
5
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