Skip to main content
OpenTrials
Completed

NCT Number: NCT04274920

Dentin Bridge Formation After Indirect Pulp Capping With Bioactive Glass Incorporated in Resin Composite and Its Adhesive in Comparison With Light Cured Calcium Hydroxide

The aim of this study is to evaluate the effect of application of bioactive glass in different protocols on the formation of dentin bridge after indirect pulp capping using resin composite with its adhesive both are containing bioactive glass.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

AlAzhar University, Faculty of Dentistry for Girls

Cairo, Egypt

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Active carious lesion in deep dentin of molars.
  • Absence of cavitated lesions at the buccal or lingual surfaces as determined by clinical and radiographic examination.
  • Absence of clinical diagnosis of pulp exposure, fistula, swelling of periodontal tissues, and abnormal tooth mobility;
  • Absence of clinical symptoms of irreversible pulpitis, such as spontaneous pain or sensitivity to pressure;
  • The extension of the carious lesion should be such that complete caries removal would risk pulp exposure, as determined by clinical and radiographic assessment;
  • Absence of radiolucencies at the interradicular or periapical regions, or thickening of the periodontal spaces, that would indicate the presence of irreversible pulp pathologies or necrosis;
  • Absence of internal or external root resorption.
  • Co-operative patients approving the trial.

Exclusion criteria

  • Patients with systemic medical conditions
  • pregnant females
  • Teeth with spontaneous pain or sensitivity to percussion.
  • Teeth with periodontal lesions, internal or external root resorption, mobility of tooth, sinus opening, or abscessed tooth.
  • Radiographic examination revealed, interrupted or broken lamina dura, widened periodontal ligament space, periapical radiolucency.

Treatment and study plan

Bioactive Glass

Other

Bioactive glass was incorporated in resin composite and its adhesive

Light cured calcium hydroxide

Other

Light cured calcium hydroxide

Primary outcomes

  1. Change of dentine thickness

    Time frame: baseline, one month, 3 months and 6 months

    Thickness in millimeters using CBCT

Sponsors and collaborators

Lead sponsor

Al-Azhar University

Other

Registry information

Official study title

Clinical Response of Human Pulps Capped With Bioactive Glass Incorporated in Resin Composite and Adhesive

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Feb 18, 2020
Registry last updated
Feb 18, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.