Restoration of Non-carious Cervical Lesions With Different Resin Composites and Universal Adhesive
Condition(s) studied
Investigational drug(s) / intervention(s)
composite restoration: different types of resin composite restorations will be used to restore NCCL
Study summary
patients with non carious cervical lesions suffer from dentin sensitivity and presence of cavitations and gingival recession. Restoring these lesions with different composites and evaluation of restorations every 6 months will be done to know the effect of different composite types and consistencies in retention of restorations of such lesions.
Eligibility
Primary outcome measure(s)
- Retention — 18-24 months
ability of resin composite restorations to be retained in the non carious cervical lesions
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Ain shams university | Cairo | Egypt | Recruiting |
More Ain Shams University trials in Egypt
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06393699 on ClinicalTrials.gov ↗ ← All trials in Egypt