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
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
Treatments tested in this trial
- composite restoration
Treatment groups
52 Participants
are divided into 4 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov