Omnia Magdy
Cairo, 02, Egypt
NCT Number: NCT02868918
The aim of this study is to compare the effect of new bioactive dentine substitute (Biodentine) versus glass ionomer cement in very deep carious lesions clinically and radiographically using digital radiography in the terms of postoperative pain and biocompatibility to the pulp.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Cairo, 02, Egypt
Roles and responsibilities:
Interventions:
Local anesthesia will be given to the patient then complete isolation to the tooth using rubber dame the operator O.M. will open the enamel Then in caries removal from the walls carbon-steel rose-head bur. Finally the deeper caries will be removed using spoon excavator
Filtek™ Z250 Universal Restorative (3M Canada, London, Ontario Canada)
-Adhesive system: Scotchbond Universal Etchant (3M ESPE, St. Paul MN, USA) & Single Bond Universal adhesive (3M ESPE, St. Paul MN, USA).
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
tricalcium silicate cement used to replace the carious dentin
Other names: tricalcium silicate
high viscosity glass ionomer used as a base material
Other names: Fuji ix
digital Xray for follow up
Other names: digital radiography
Time frame: 6 months
Time frame: 6 months
Cairo University
Other
Clinical and Radiographical Evaluation of New Bioactive Dentine Substitute (Biodentine) Versus Glass Ionomer Cement in Treatment of Very Deep Carious Lesions -Randomized Clinical Trial
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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.
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