Skip to main content
Clinical Trials/NCT04572386
NCT04572386
Unknown
Not Applicable

Clinical Performance of Low Technique Sensitive Self-cured Universal Adhesive Versus Light Cured Universal Adhesive in Patients With Non-carious Cervical Lesions (NCCLs): 18 Month Randomized Clinical Trial

Aya Gamal ashour0 sites28 target enrollmentOctober 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non Carious Cervical Lesion
Sponsor
Aya Gamal ashour
Enrollment
28
Primary Endpoint
number of restoration with retention loss
Last Updated
5 years ago

Overview

Brief Summary

This study will be conducted to evaluate the clinical performance of self-cured adhesive versus light cured universal adhesive in non-carious cervical lesions (NCCL) resin composite restorations after 18 month

Registry
clinicaltrials.gov
Start Date
October 2020
End Date
July 2022
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Aya Gamal ashour
Responsible Party
Sponsor Investigator
Principal Investigator

Aya Gamal ashour

principle investigator

Cairo University

Eligibility Criteria

Inclusion Criteria

  • particepant with age rang 18-55
  • particepant with non carious cervical lesion

Exclusion Criteria

  • particepant outside age rang
  • particepant with periodontal problem that might affect the teeth to be treated

Outcomes

Primary Outcomes

number of restoration with retention loss

Time Frame: 18-month

Frist visual evaluation to ensure that there is no complete loss of retention of the restoration then tactile evaluation will be done using probe tip that will be held gently at right angle to the labial surface and move from restoration to tooth and vice versa to insure no rocking /fracture /ditching in the restoration following FDI criteria

Number of fracture restoration

Time Frame: 18 month

Frist visual evaluation to ensure that there is no complete loss of retention of the restoration then tactile evaluation will be done using probe tip that will be held gently at right angle to the labial surface and move from restoration to tooth and vice versa to insure no rocking /fracture /ditching in the restoration following FDI criteria ( first visually for total loss .followed by tactile inspection using fdi prob for any fracture /rocking or loss of retention

Secondary Outcomes

  • Number of restoration with change in colour or texture(18 month)
  • Number of restoration caused biological harm(18 month)

Similar Trials