Root Coverage Performance of Restorative Materials in Class V Cavities

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorZeliha Başak Çakır Erdil

About this trial

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 criteria

Qualifiers

None

Disqualifiers

Age younger than 18 years. Pregnancy or breastfeeding. Poor oral hygiene. Uncontrolled systemic disease or any medical condition contraindicating periodontal surgery.

Trial design

Treatments tested in this trial

  • No Restoration Control Group
  • Glass Ionomer Cement Group
  • Resin Composite Group

Treatment groups

30 Participants
are divided into 3 treatment groups

Sponsors and collaborators

Zeliha Başak Çakır Erdil

Lead sponsor

Adiyaman University

Sponsor institution