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Proximal Caries clinical trials

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NCT ID: NCT04776785 Completed - Proximal Caries Clinical Trials

Effect of Self-Assembling Peptides on the Progression of Non-Cavitated Proximal Caries

Start date: October 1, 2019
Phase: N/A
Study type: Interventional

The aim of this randomized controlled, double-blinded, split-mouth clinical trial was to evaluate the efficacy of self-assembling peptide P11-4 solution (Curodontâ„¢ Repair) with fluoride varnish on the progression of non-cavitated proximal caries compared to casein phosphopeptide-amorphous calcium phosphate (CPP-ACP) with fluoride varnish (MI Varnishâ„¢) sodium fluoride (NaF) varnish (Profluorid® Varnish). The study included 300 permanent molars belonging to 150 children, aged between 7 to 13 years old, who had two non-cavitated proximal carious lesions.

NCT ID: NCT04677023 Not yet recruiting - Proximal Caries Clinical Trials

Evaluation of Organically Modified Ceramic Resin Composite Versus Bulkfill Resin in Proximal Posterior Cavities

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

In patients with compound posterior proximal cavities, will the use of organically modified ceramic resin composite restorative material have similar clinical performance to conventional bulk fill resin composite, evaluation of restorations will be done at baseline,six and twelve months using World Dental Federation FDI criteria.

NCT ID: NCT02191943 Withdrawn - Proximal Caries Clinical Trials

Lesion Progression of Approximal Caries After Resin Infiltration

Start date: November 2014
Phase: N/A
Study type: Interventional

The aim of the planned in-vivo trial is to investigate the effectiveness of the caries infiltration technique for the repression of caries progression. Within the framework of this investigation it is intended that the hypothesis to be substantiated is that carious cavities, which have been treated with the caries infiltration technique, exhibit significantly reduced radiological progression than those cavities that have been treated using standard preventive treatments. In this multicenter trial, a total of 90 test subjects are included and 45 test subjects at each institution are to be treated with both, the infiltration technique and using conventional fluoridation treatment in different sides of the mouth ("split-mouth design"). The anticipated result of this trial shall deliver information on the long-term effectiveness of caries infiltration to prevent the progression of existing approximal carious lesions, and thereby enable an improvement in caries prevention within the scope of dental treatment.

NCT ID: NCT01224925 Completed - Reversible Pulpitis Clinical Trials

RCT of Pulp Capping Over Carious Exposure in Adults

Start date: October 18, 2010
Phase: N/A
Study type: Interventional

This multicentre study was a randomized, controlled, parallel, patient-blinded, two-arm superiority trial with a 1:1 allocation ratio that followed the CONSORT guidelines.The aim of this study was to investigate whether MTA is more effective than a conventional calcium hydroxide liner (Dycal®) as a direct pulp capping material in mature molar teeth with a carious pulpal exposure.