Clinical Evaluation of Four Aesthetic Restorations in Non-carious Cervical Lesions

Noncarious Cervical Lesions Clinical Trial

Official title:
Clinical Evaluation of Four Aesthetic Restorations in Non-carious Cervical Lesions: a Randomised Controlled Split-mouth Clinical Trial

Status Withdrawn

Clinical Trial Summary

To compare the clinical performance of high-viscosity glass ionomer, flowable composite, bulkfill composite and nanohybrid composite restorations in non-carious cervical lesions (NCCLs).

Clinical Trial Description

One hundred fourty NCCLs were randomised into four groups according to a split-mouth design. Clinical evaluations will be performed after 1 week, 3 months, 6 months, using FDI (World Dental Federation) criteria. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04261140
Study type	Interventional
Source	Recep Tayyip Erdogan University Training and Research Hospital
Contact
Status	Withdrawn
Phase	N/A
Start date	July 2019
Completion date	May 2021

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See also
Status	Clinical Trial	Phase
Active, not recruiting	`NCT03713827` - Clinical Performance of a Glass Hybrid Restorative in NCCL's of Patients With Bruxism	N/A
Completed	`NCT00867997` - Noncarious Cervical Lesion Treatment Outcomes	Phase 3
Recruiting	`NCT05533255` - Preheated Composites Vs. Conventional Composites in Noncarious Cervical Lesions	N/A