Restoration of Non-carious Cervical Lesions With Different Resin Composites and Universal Adhesive

ConditionRetention

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age18-65

SponsorAin Shams University

About this trial

patients with non carious cervical lesions suffer from dentin sensitivity and presence of cavitations and gingival recession. Restoring these lesions with different composites and evaluation of restorations every 6 months will be done to know the effect of different composite types and consistencies in retention of restorations of such lesions.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Presence of at least 2 NCCLs in one side.

Patients with no medical condition could interfere with the routine dental care.

Patients who will be able to attend for each recall visit.

Patients with healthy periodontal tissues.

Disqualifiers

Medically compromised patients.

Pregnant or breast-feeding patients.

Patients undergoing orthodontic treatment or bleaching treatment in the time of the study.

Patients with periodontal disease in the target area.

Trial design

Design model

Parallel

Treatments tested in this trial

composite restoration
Procedure/Surgery
different types of resin composite restorations will be used to restore NCCL

Treatment groups

52 Participants

are divided into 4 treatment groups

Group A: incrementalExperimental treatment 1 intervention

Group B: bulk fill heatedExperimental treatment 1 intervention

Group C: incremental heatedExperimental treatment 1 intervention

Group D: flowableExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

Retention

ability of resin composite restorations to be retained in the non carious cervical lesions

Time frame

18-24 months

Secondary outcomes

marginal staining

will be assessed visually by blinded evaluator

Time frame

18-24 months

Other outcomes

Marginal adaptation

will be assessed by explorer done by blinded evaluator

Time frame

18-24 months

postoperative sensitivity

will be assessed using triple way syringe with air done by blinded evaluator

Time frame

18-24 months

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Ain Shams University

Lead sponsor

Source ClinicalTrials.gov

Apply now