Clinical Performance and Antibacterial Effect of Alkasite Bioactive Material in Restoring Pulpotomized Primary Molars

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age5-9
SponsorNoha Fouad

About this trial

The study aims to evaluate the clinical performance of Cention-Forte (CF) material in the restoration of pulpotomized second primary molars compared to conventional stainless steel crowns (SSC), and also to assess the restorations' antibacterial effect on salivary cariogenic bacterial count.

Eligibility criteria

Qualifiers

Cooperative children (Positive or definitely positive) according to the Frankl's behaviour rating scale.

Children free of any systemic disease or special health care needs (ASA1).

Completion of an informed consent to participate in the study.

Second primary molar tooth with occluso-proximal carious lesions indicated for pulpotomy.

Disqualifiers

Clinical signs or symptoms of irreversible pulpitis or non- vitality.

Radiographic signs of degeneration including internal or external root resorption, furcation involvement.

Pathologic mobility detected by placing the points of a pair of tweezers in the occlusal fossa and gently rocking the tooth buccolingually.

Reported usage of local or systemic antibiotics, chlorhexidine or fluoride mouthwashes within the last 2 weeks.

Trial design

Treatments tested in this trial

  • Cention Forte alkasite bioactive restorative material
  • Stainless steel crown

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Noha Fouad

Lead sponsor

Alexandria University

Sponsor institution