18-Month Clinical Evaluation of Self-Adhesive Flowable Giomer Compared to Conventional Flowable Giomer in Carious Cervical Lesions: A Randomized Clinical Trial

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCairo University

About this trial

The material under investigation will offer the patient a high strength and high durability restoration with the advantage of having anti-bacterial properties.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Cervical carious lesions in anterior teeth and premolars

Small to moderate class V carious lesion (ICDAS 3 & 4).

Vital upper or lower periodontally sound teeth with no signs of irreversible pulpitis.

Presence of favorable occlusion and teeth are in normal contact with the adjacent teeth

Disqualifiers

Cervical carious lesions in molars.

Deep carious defects (close to pulp, less than 1 mm distance).

Teeth with clinical symptoms of pulpitis such as spontaneous pain or sensitivity to pressure.

Non-vital teeth, Fractured or cracked teeth.

Trial design

Design model

Parallel

Treatments tested in this trial

  • FIT SA

    Other intervention

    self-adhesive flowable giomer restorative material

  • Beautifil Flow Plus F00

    Other intervention

    Conventional flowable giomer restorative material

Treatment groups

34 Participants
are divided into 2 treatment groups
Group A: Beautifil Flow Plus F00Active comparator 1 intervention
Group B: FIT SAExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Clinical Performance

Clinical Performance using Modified USPHS criteria

Time frame
18 months

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: