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18-Month Clinical Evaluation of Self-Adhesive Flowable Giomer Compared to Conventional Flowable Giomer in Carious Cervical Lesions: A Randomized Clinical Trial

Not Applicable
Not yet recruiting
Conditions
Cervical Caries
Registration Number
NCT06946134
Lead Sponsor
Cairo University
Brief Summary

The material under investigation will offer the patient a high strength and high durability restoration with the advantage of having anti-bacterial properties.

Detailed Description

There is no available evidence for assessing FIT SA restorative material in restoration of cervical lesions. Therefore, this study aims to provide valuable insights into the shear bond strength and clinical performance, in terms of the biological, mechanical and esthetic parameters, of FIT SA restorative material in restoration of cervical lesions.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
34
Inclusion Criteria
  1. Cervical carious lesions in anterior teeth and premolars
  2. Small to moderate class V carious lesion (ICDAS 3 & 4).
  3. Vital upper or lower periodontally sound teeth with no signs of irreversible pulpitis.
  4. Presence of favorable occlusion and teeth are in normal contact with the adjacent teeth
Exclusion Criteria
  1. Cervical carious lesions in molars.
  2. Deep carious defects (close to pulp, less than 1 mm distance).
  3. Teeth with clinical symptoms of pulpitis such as spontaneous pain or sensitivity to pressure.
  4. Non-vital teeth, Fractured or cracked teeth.
  5. Endodontically treated teeth.
  6. Periodontally affected teeth

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Clinical Performance18 months

Clinical Performance using Modified USPHS criteria

Secondary Outcome Measures
NameTimeMethod

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