Comparison of the Functional Properties of Two Injectable Materials in Posterior Teeth: Randomized Clinical Trial

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-50
SponsorFuture University in Egypt

About this trial

Using two different injectable materials in class II cavities to compare functional properties

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

1-Adult patients (20-50) 2-Good oral hygiene Good oral hygiene (Plaque index ≤2 (Moderate accumulation with plaque in the sulcus)) 3-Patient approval 4-Absence of parafunctional habits and/or bruxism 5-No endodontic treatment or abscess 6- class II either mesial or distal (no MOD cavities)

Disqualifiers

1. Systematic disease that may affect participation. 2. Xerostomic patients. 3. Bad oral hygiene (plaque index 2 or 3) 14 4. Heavy smokers 5. Patients undergoing or will start orthodontic treatment 6. Signs and symptoms of irreversible pulpitis.

Trial design

Design model

Single group

Treatments tested in this trial

  • Gaenial universal injectable

    Other intervention

    GC Gaenial universal injectable advanced injectable composite with nano sized filler that merge the adaptation of flowable composite and mechanical properties of hybird composite

Treatment groups

52 Participants
are divided into 1 treatment group
Group A: beautiful flow plus xExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Marginal adaptation

Time frame
T1: 1week T2: 6months T3 12 months
2

1- fracture of restoration and retention 2- proximal contact poiont

Time frame
T(Time) T1:1 week hours beasline T2: 6 months T3:12 months

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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