Actively Recruiting
Clinical Evaluation of Self-Adhesive Bulk-Fill Composite Versus Conventional Nano-hybrid Composite in Cervical Cavities
Led by Misr International University · Updated on 2024-07-08
54
Participants Needed
1
Research Sites
72 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this randomized clinical trial is to compare the six months clinical performance of the self-adhesive bulk-fill composite with the conventional nano-hybrid composite in the cervical lesions of teeth in the esthetic zone. In addition, to evaluate patient's satisfaction towards the self-adhesive bulk-fill material and its total operatory time.
CONDITIONS
Official Title
Clinical Evaluation of Self-Adhesive Bulk-Fill Composite Versus Conventional Nano-hybrid Composite in Cervical Cavities
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Cervical lesions
- Cervical lesions at least 1 mm deep including enamel and dentin
- Cervical lesions not deeper than 3 mm
- Male or female gender
- Medically free patients
- Normal occlusion
- Healthy gingiva
You will not qualify if you...
- Teeth with signs of pulpitis or periapical disease
- Patients older than 60 years
- Patients younger than 18 years
- Pregnant women
- History of allergy to resin materials
- Patients with disabilities
- Cervical lesions extending to proximal surfaces
- Lesions on palatal or lingual surfaces
- Teeth with root caries
- Teeth that have had root canal treatment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Misr International University
Cairo, Egypt, 11223344
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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