Clinical Evaluation of Self- Cure Bulk-Fill Resin Composite Versus Conventional Bulk-Fill Resin Composite Versus Conventional Bulk-Fill Resin Composite Clinical Evaluation of Self- Cure Bulk-Fill Resin Composite Versus Conventional Bulk-Fill Resin Composite

ConditionProximal Cavities of Posterior Teeth

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age18-100

SponsorCairo University

About this trial

the aim of this study is To evaluate and compare the clinical performance of Self- Cure Bulk fill Composite Resin Versus Conventional Bulk fill resin composite in Restoration of Proximal Lesions over a Period of 24 months Follow-up.

Eligibility criteria

Qualifiers

Patients consulting in one of the outpatient clinics listed above.

Able to tolerate necessary restorative procedures.

Provide informed consent.

Accepts the 18 months follow-up period.

Disqualifiers

Medically compromised patients, as they will not be able to attend multiple appointments or may require special management.

Pregnant women; as radiographs cannot be taken for them.

Allergy to any of the restorative materials, including anesthetics.

Uncooperative patients, will not abide by the instructions or attend the appointments.

Trial design

Treatments tested in this trial

class II restoration

Treatment groups

56 Participants

are divided into 2 treatment groups

Locations

Cairo University Cairo Egypt

Sponsors and collaborators

Cairo University

Lead sponsor

Source ClinicalTrials.gov