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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04324008
Other study ID # Flowable composites
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date November 1, 2017
Est. completion date November 1, 2024

Study information

Verified date April 2024
Source Hacettepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate a self-adhesive flowable resin composite, a flowable resin composite with high viscosity and a conventional flowable resin composite in combination with a universal adhesive using two different application modes. All patients will receive at least 4 occlusal restorations. Cavities will be divided into four groups according to restorative systems used: Constic (a self-adhering flowable composite), G-ænial Universal Flo (a highly filled flowable composite), Tetric N-Flow (self-etch) (a conventional flowable composite), Tetrin N-Flow (etch&rinse).


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 28
Est. completion date November 1, 2024
Est. primary completion date January 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - having no medical or behavioral problems preventing then from attending review visits - absence of previously placed restorations - having antagonist teeth Exclusion Criteria: - poor gingival health - uncontrolled, rampant caries - bruxism - removable partial dentures - xerostomia

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Constic
Flowable resin composite
G-ænial Universal Flo
Flowable resin composite
Tetric N-Flow (self-etch)
Tetric N-Flow (Tetric N-Bond Universal, self-etch mode)
Tetric N-Flow (etch&rinse)
Tetric N-Flow (Tetric N-Bond Universal, etch&rinse mode)

Locations

Country Name City State
Turkey Hacettepe University Ankara

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical performances of different flowable resin composite Two year results according to USPHS criteria two years
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