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

NCT06991582 · Status: NOT_YET_RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2025-05-28

No results posted yet for this study

Summary

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

Conditions

  • Carious Primary
  • Carious Anteriors

Interventions

BIOLOGICAL

Injectable composite resin restoration

Injectable composite Beautifil flow Plus X (Shofu INC., Koyoto, Japan)

BIOLOGICAL

packable composite

Packable Composite Beautifil II (Shofu INC., Koyoto, Japan)

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-05-28
Primary Completion
2026-02-28
Completion
2026-03-30

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 NCT06991582 on ClinicalTrials.gov