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Clinical Assessment of Injectable Composite Versus Packable Composite in Treatment of Carious Primary Anterior Teeth

Cairo University (CU) logo

Cairo University (CU)

Status and phase

Not yet enrolling
Phase 2

Conditions

Carious Primary
Carious Anteriors

Treatments

Biological: Injectable composite resin restoration
Biological: packable composite

Study type

Interventional

Funder types

Other

Identifiers

NCT06991582
14422023595700

Details and patient eligibility

About

The aim of this study is to evaluate the clinical success of injectable composite versus packable composite in restoration of primary anteriors.

Enrollment

16 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children with caries in primary anterior teeth.
  • Caries involving class III, IV, V or multisurface caries
  • Restorable anterior teeth
  • Pre operative Radiograph showing at least half of the root is not resorbed).

Exclusion criteria

  • Badly decayed non restorable anterior teeth
  • Signs and symptoms of root resorption (more than half the root is resorbed)
  • Presence of bony resorption
  • Presence of pathological root resorption
  • Tooth Mobility

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

16 participants in 2 patient groups

Injectable composite
Experimental group
Description:
Injectable composite Beautifil flow Plus X (Shofu INC., Koyoto, Japan)
Treatment:
Biological: Injectable composite resin restoration
Packable Composite
Active Comparator group
Description:
Packable Composite Beautifil II (Shofu INC., Koyoto, Japan)
Treatment:
Biological: packable composite

Trial contacts and locations

1

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Central trial contact

Bassant Mohamed ElMesbahy

Data sourced from clinicaltrials.gov

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