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Evaluation of Adhering Flowable Composite With and Without Adhesive Vs Flowable in Cervical Lesions

NCT03859284 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2020-10-29

No results posted yet for this study

Summary

With limited evidence-based information in literature about using self-adhering flowable composite in conservative class V restorations, it was found beneficial to evaluate the newly introduced material using a randomized controlled clinical trial to test the null hypothesis that moist bonding self-adhering flowable composite with and without adhesive system will have the same clinical performance as conventional flowable composite in cervical caries lesions.

Conditions

  • Dental Restoration Failure

Interventions

OTHER

flowable resin composite

gold standard

OTHER

self adhering flowable

moist bonding self adhering flowable composite

OTHER

self adhering flowable with adhesive

moist bonding self adhering flowable composite with the aid of an adhesive system.

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
16 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-06-20
Primary Completion
2021-02-28
Completion
2022-06-01

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03859284 on ClinicalTrials.gov