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Search / Trial NCT06348953

Bioactive Versus Non-Bioactive Restorative System in Deep Carious Molars

Launched by CAIRO UNIVERSITY · Mar 29, 2024

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Self Etch Adhesive Deep Caries In Permanent Molars Bioactive Restorative System Selective Caries Removal Partial Caries Removal Selective Removal To Soft Caries Bioactive Adhesive Bioactive Bond Bioactivity Deep Carious Molars Rct

ClinConnect Summary

This clinical trial is exploring how different types of dental materials—specifically bioactive and non-bioactive restorative systems—affect the treatment of deep cavities in permanent back teeth (molars). The researchers want to understand which material works better after a method called selective caries removal, which aims to keep as much healthy tooth as possible while removing decay. They will look at how well the restorations hold up over time, how they affect the tooth's health, and the overall success of the treatments.

To participate in this study, individuals aged 18 to 40 who have a specific type of deep cavity in their back teeth may be eligible. Candidates must be able to handle the necessary dental procedures and agree to follow-up appointments. However, those with allergies to dental materials, pregnant women, or individuals with certain dental or medical conditions may not qualify. Participants can expect to receive care for their cavities while contributing to valuable research that could improve future dental treatments.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • young adult patients (age: 18-40 years) of both genders.
  • Able to tolerate necessary restorative procedures.
  • Willing to sign the informed consent.
  • Accepts the follow-up period.
  • Posterior permanent tooth with occlusal proximal deep carious lesion.
  • Radiographically (bitewing radiograph) extending to the inner 1/3 of dentine (D3) with a radiopaque layer between the carious lesion and the pulp chamber.
  • Sensible teeth according to cold pulp test.
  • Exclusion criteria:
  • Allergy to any restorative materials.
  • Patients undergoing orthodontic treatment with fixed appliances.
  • Pregnant women.
  • Patients with debilitating systemic diseases
  • Teeth with previous restorations.
  • Spontaneous pain or prolonged pain (more than 15 s) after sensitivity test (cold test), which would indicate irreversible pulpitis.
  • Negative sensibility tests, periapical radiolucencies and sensitivity to axial or lateral percussion.
  • Mobile teeth, indicating periodontal disease or trauma.
  • External or internal resorption.
  • Cervical carious lesions.

About Cairo University

Cairo University, a premier institution in Egypt, is dedicated to advancing medical research and education through innovative clinical trials. With a strong emphasis on improving healthcare outcomes, the university collaborates with various stakeholders to conduct rigorous scientific studies that address critical health challenges. Leveraging its extensive resources and expert faculty, Cairo University aims to contribute valuable insights to the medical community and enhance patient care both locally and globally. Through its commitment to ethical research practices and excellence, the university plays a pivotal role in shaping the future of healthcare in the region.

Locations

Cairo, , Egypt

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported