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
Sponsors and collaborators
Zeliha Başak Çakır Erdil
Lead sponsor
Adiyaman University
Sponsor institution