Clinical Evaluation of Self-Adhesive Bulk-Fill Composite Versus Conventional Nano-hybrid Composite in Cervical Cavities
Recruiting
N/A
Interventional Study
Cervical Caries
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 60
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 54 (estimated)
- Sponsor
- Misr International University · Other
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About This Trial
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Cervical lesions.
* Cervical lesions of at least one mm depth; to include enamel and dentin.
* Cervical lesions of not more than 3 mm in depth.
* Male or female genders.
* Medically free patients.
* Normal occlusion.
* Healthy Gingiva
Exclusion Criteria:
* Teeth showing sign…
Contacts
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