Actively Recruiting
Color Stability and Wear Resistance of Direct Flowable and Preheated Composite Using the Injectable Technique
Led by King Abdullah University Hospital · Updated on 2024-08-06
142
Participants Needed
1
Research Sites
626 weeks
Total Duration
On this page
Sponsors
K
King Abdullah University Hospital
Lead Sponsor
J
Jordan University of Science and Technology
Collaborating Sponsor
AI-Summary
What this Trial Is About
The aim of this study is to conduct the first clinical trial to assess the color stability and wear resistance of the highly filled injectable flowable composite materials compared to preheated conventional ones and evaluate the in vivo performance of the injectable composite technique.
CONDITIONS
Official Title
Color Stability and Wear Resistance of Direct Flowable and Preheated Composite Using the Injectable Technique
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients older than 18 years
- Asymptomatic sound anterior teeth, or localized Class III/IV/V cavity or restoration
- Patients with irregular tooth anatomies, misalignments, spacing, mild staining, cervical wear that are indicated for direct composite veneers
- Restorations in functional occlusions with an opposing natural tooth
- Two proximal contacts area with neighboring teeth
You will not qualify if you...
- Patients with contra-indications for regular dental treatment based on their medical history
- Patients at a high risk of caries
- Patients with poor oral hygiene
- Teeth with compromised periodontal status
- Evidence of active parafunctional habits or excessive tooth wear
- Severe discoloration
- Heavy smokers
- Patients with special aesthetic requirements that could not be solved by direct composite veneers
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Jordan University of Science and Technology
Irbid, Jordan, P.O.Box 3030
Actively Recruiting
Research Team
G
Ghada A Maghaireh
CONTACT
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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