Evaluation of Adhering Flowable Composite With and Without Adhesive Vs Flowable in Cervical Lesions

Last updated: October 27, 2020
Sponsor: Cairo University
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT03859284
Mon15
  • Ages 16-55
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

With limited evidence-based information in literature about using self-adhering flowable composite in conservative class V restorations, it was found beneficial to evaluate the newly introduced material using a randomized controlled clinical trial to test the null hypothesis that moist bonding self-adhering flowable composite with and without adhesive system will have the same clinical performance as conventional flowable composite in cervical caries lesions.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • patients with anterior cervical carious lesions.
  • Pulp asymptomatic vital carious anterior teeth.
  • Co-operative patients approving to participate in the trial.

Exclusion

Exclusion Criteria:

  • Pregnancy.
  • Disabilities.
  • Systemic disease or severe medical complications.
  • Deep extensive carious cavities that may lead to the fracture of the tooth or pulpalaffection.
  • Teeth with signs and symptoms of irreversible pulpitis or pulp necrosis.
  • Heavy smokers.

Study Design

Total Participants: 45
Study Start date:
June 20, 2020
Estimated Completion Date:
June 01, 2022

Study Description

flowable composite is considered a gold standard in class V restorations due to its resilient character the prevents its dislodgement in this area. self-adhering flowable composite would simplify the clinical steps and claims to improve the adhesion.

Connect with a study center

  • Faculty of Dentistry Cairo University

    Giza,
    Egypt

    Active - Recruiting

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