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Clinical Evaluation of Different Universal Adhesive Systems in Non-carious Cervical Lesions.

NCT04707898 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2021-01-13

No results posted yet for this study

Summary

The aim of the study is to compare the performance of universal adhesives containing different-solvent-based in the restoration of non-carious cervical lesions (NCCLs).

Conditions

  • Non-carious Cervical Lesions

Interventions

DEVICE

Single Bond Universal

Adhesive system

DEVICE

G-Premio Bond

Adhesive system

Sponsors & Collaborators

  • Okan University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-10-15
Primary Completion
2022-10-15
Completion
2022-11-15

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04707898 on ClinicalTrials.gov