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Clinical Trials/NCT04720638
NCT04720638
Unknown
Not Applicable

Clinical Performance of Short Fiber Reinforced Flowable Resin Composite Restorations Versus Conventional Resin Composite Restorations in Posterior Teeth (2y Randomized Clinical Trial)

Cairo University1 site in 1 country70 target enrollmentStarted: March 2021Last updated:

Overview

Phase
Not Applicable
Enrollment
70
Locations
1
Primary Endpoint
Clinical performance (Alpha is the best score, bravo, charlie the worst score)

Overview

Brief Summary

Clinical performance of short fiber reinforced flowable resin composite restorations versus conventional resin composite restorations will be tested in posterior teeth (2y randomized clinical trial).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
17 Years to 55 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Patients with large proximal carious cavities in molars.
  • Pulp asymptomatic vital carious upper or lower molars.
  • Good oral hygiene.

Exclusion Criteria

  • Presence of signs and symptoms of irreversible pulpitis or pulp necrosis
  • Severe medical complications.
  • Allergic history concerning methacrylates
  • Evidence of parafunctional habits.

Outcomes

Primary Outcomes

Clinical performance (Alpha is the best score, bravo, charlie the worst score)

Time Frame: Change from baseline at 6, 12 ,18, 24 months

Modified USPHS criteria; . Post operative Hypersensitivity Secondary caries Gross fracture Color match Cavo-surface marginal discoloration Marginal integrity Proximal contact

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Rawda Hesham Abd ElAziz

lecturer

Cairo University

Study Sites (1)

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