NCT07687654 Root Coverage Performance of Restorative Materials in Class V Cavities
| NCT ID | NCT07687654 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Zeliha Başak Çakır Erdil |
| Condition | Gingival Recession |
| Study Type | INTERVENTIONAL |
| Enrollment | 30 participants |
| Start Date | 2025-11-20 |
| Primary Completion | 2026-08 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 30 participants in total. It began in 2025-11-20 with a primary completion date of 2026-08.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief 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 Criteria
Inclusion Criteria: Adults aged 18 years or older. Patients presenting with Cairo RT1 (Miller Class I or II equivalent) gingival recession defects requiring root coverage surgery. Presence of a non-carious cervical lesion (NCCL), an existing cervical restoration, or a cervical defect requiring restoration. Cervical lesion depth of ≤1.5 mm. Patients who have completed initial periodontal therapy before enrollment. Good oral hygiene (Plaque Index ≤20% or as determined by the investigator). Indication for root coverage surgery with a subepithelial connective tissue graft. Teeth suitable for restoration with glass ionomer cement, resin composite, or flowable resin composite, or requiring no restoration according to the study protocol. Ability and willingness to provide written informed consent and comply with study visits. Exclusion Criteria: * Age younger than 18 years. Pregnancy or breastfeeding. Poor oral hygiene. Uncontrolled systemic disease or any medical condition contraindicating periodontal surgery. Bleeding disorders or current anticoagulation that contraindicates connective tissue graft harvesting. Known allergy or hypersensitivity to resin composite, flowable resin composite, glass ionomer cement, or any study materials. Patients who have not completed initial periodontal therapy. Cervical lesions deeper than 1.5 mm. Conditions that, in the investigator's opinion, could interfere with wound healing, periodontal surgery, or study outcomes.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07687654 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Gingival Recession. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07687654 currently recruiting?
Yes, NCT07687654 is actively recruiting participants. Contact the research team at bskcakirr@gmail.com for enrollment information.
Where is the NCT07687654 trial being conducted?
This trial is being conducted at Adıyaman, Turkey (Türkiye).
Who is sponsoring the NCT07687654 clinical trial?
NCT07687654 is sponsored by Zeliha Başak Çakır Erdil. The trial plans to enroll 30 participants.