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Clinical Trials/NCT06226389
NCT06226389Active, not recruitingNot Applicable

2-Year Clinical Evaluation of Different Bulk-fill Resin Composite Restorative Systems in Posterior Teeth

Mansoura University1 site in 1 country40 target enrollmentStarted: January 17, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
40
Locations
1
Primary Endpoint
Difference between baseline and after 2 years of evaluation of resin based composite

Study Overview

Brief Summary

Different bulk-fill composites will be applied in different posterior cavities then compared

Detailed Description

Patients must be in middle age(25-55) age,able to regularly follow up,not pregnant and at least have 4 carious molars

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
25 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •at least 4 carious molars

Exclusion Criteria

  • •pregnancy patient
  • •Not able to regularly follow up
  • •bad oral hygiene

Arms & Interventions

4 Different bulk-fill composite

Experimental

Bulk-fill composite will be applied in different 4 posterior cavities with 3-4 ml in depth

Intervention: 4 different bulk-fill composite (Procedure)

Aging

Experimental

For long term follow up

Intervention: 4 different bulk-fill composite (Procedure)

Outcomes

Primary Outcomes

Difference between baseline and after 2 years of evaluation of resin based composite

Time Frame: Baseline to 2 years

Change in FDI criteria

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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