RecruitingNot Applicable

Effect of Aging on Micro-tensile Bond Strength and Color Stability of Self-adhesive Resin Composite

Egypt20 participantsStarted 2024-06

Plain-language summary

The objective of this study is to evaluate the micro-tensile bond strength of a newly self-adhesive resinous restorative material to dentin with and without application of universal bonding system (in-vitro) and to examine it's clinical performance by evaluation of it's color stability and marginal discoloration through a randomized clinical trial (in-vivo).

Who can participate

Age range25 Years – 45 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients with class I lesion in their maxillary or mandibular molars with a maximum of approximately 2 mm final cavity depth. * Patients with teeth shade A2 according to Vitapan classical shade guide. * Patients with an acceptable oral hygiene level. * Patients keen to regularly attend the follow up visits. Exclusion Criteria: * Patients with heavy bruxism or traumatic occlusion. * Patients with poor oral hygiene or active periodontal disease. * Patients with exposed or endodontically treated teeth. * Patients participated in a clinical trial within 6 months before beginning of this trial. * Patients who decline to be involved in the study or sign the written consent. * Patients unable to return for the follow up visits.

What they're measuring

Clinical evaluation of color stability and marginal discoloration of resin restorations after aging in the patient mouth.

Timeframe: 6 months

Trial details

NCT IDNCT06463574

SponsorMinia University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-11

Contact for this trial

Nourhan Samir Soliman, Assisstant Lecturer

1066175951 nourhan.samir@pua.edu.eh

View on ClinicalTrials.gov More Tooth Decay trials