Evaluation of Using Self-adhering Flowable Resin Composite in Repairing Old Defective Resin Composite Restorations Over 18 Months Follow up. (A Randomized Clinical Trial)

NCT ID: NCT06260644

Last Updated: 2024-02-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

34 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-02-01

Study Completion Date

2025-10-31

Brief Summary

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This research proposal is evaluating the clinical performance of using self-adhering flowable resin composite in repairing old occlusal defective resin composite versus conventional flowable resin composite restoration over 18 months.

Detailed Description

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Conditions

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Occlusal Caries

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

parallel assignment
Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors
double ( participants, outcomes assessor) participants and both assessors will be blind to the type of material used

Study Groups

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Conventional flowable nano filled resin composite

Repairing the old defective class I composite restoration by conventional nano filled flowable resin composite.

Group Type ACTIVE_COMPARATOR

VertiseTM flowable composite (Kerr,USA)

Intervention Type PROCEDURE

self adhesive flowable resin composite restoration.

Self adhesive flowable resin composite

Repairing the old defective class I composite restoration by self adhering flowable resin composite.

Group Type EXPERIMENTAL

VertiseTM flowable composite (Kerr,USA)

Intervention Type PROCEDURE

self adhesive flowable resin composite restoration.

Interventions

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VertiseTM flowable composite (Kerr,USA)

self adhesive flowable resin composite restoration.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients (18-35 y)
* patients with defective resin composite class I restorations that need repair.
* dental motivated patients who attends regularly.
* Vital posterior teeth with repairable defective resin composite class I restorations.
* Localized marginal defect or marginal staining FDI 3\& 4.
* Teeth with no or minimum mobility \& healthy peridontium.
* No history of any irreversible pulpal pain or necrosis in the teeth to be restored.

Exclusion Criteria

* • Patients with defective restorations that dictate replacement

* Uncooperative behavior limits the isolation techniques throughout the procedure.
* Presence of parafunctional habits.
* Patient with history of systemic medical disease, or any other serious relevant problem.
* High caries risk patients. Periodontal disease that may affect the prognosis of the restoration or the tooth itself.
* Fractured or visibly cracked teeth.
* Symptoms of any pulp pathosis.
* Defective resin composite restorations that dictate replacement.
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Soha Sayed Hosny

masters degree student

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Faculty of Dentistry

Cairo, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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Repairing defective composite

Identifier Type: -

Identifier Source: org_study_id

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