RecruitingNot ApplicableNCT07687654

Root Coverage Performance of Restorative Materials in Class V Cavities

Clinical Evaluation of the Root Coverage Performance of Different Restorative Materials in Class V Cavities in Patients With Gingival Recession


Sponsor

Zeliha Başak Çakır Erdil

Enrollment

30 participants

Start Date

Nov 20, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This prospective randomized controlled clinical trial aims to evaluate the influence of different restorative materials placed in Class V cervical lesions on the clinical outcomes of root coverage surgery using a subepithelial connective tissue graft. Patients with Cairo RT1 (Miller Class I-II equivalent) gingival recession associated with non-carious cervical lesions or existing cervical restorations will receive one of the restorative approaches according to the study protocol. Clinical parameters, including the percentage of root coverage and soft tissue stability, will be evaluated during follow-up to determine which restorative approach provides the most favorable clinical outcome.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Glass Ionomer Cement Group, a procedure called No Restoration Control Group, and others for people with gingival recession and non-carious cervical lesions (nccls). The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 65 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDURENo Restoration Control Group

No restorative material will be placed in the Class V cervical lesion before root coverage surgery. Participants will undergo root coverage surgery using a coronally advanced flap with a subepithelial connective tissue graft according to the study protocol.

DEVICEGlass Ionomer Cement Group

A conventional glass ionomer cement was used to restore the Class V cervical lesion before root coverage surgery with a subepithelial connective tissue graft.

DEVICEResin Composite Group

A resin composite material was used to restore the Class V cervical lesion before root coverage surgery with a subepithelial connective tissue graft.


Locations(1)

Faculty of Dentistry, Adıyaman University

Adıyaman, Merkez, Turkey (Türkiye)

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NCT07687654


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