Skip to main content
Clinical Trials/NCT02994862
NCT02994862UnknownNot Applicable

One Year Clinical Evaluation of E. Max Laminate Veneers With and Without Using Galla Chinnesis as Natural Cross Linking and Remineralizing Agent Before Bonding to Teeth With Amelogenesis Imperfecta

Cairo University0 sites16 target enrollmentStarted: December 2016Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
16
Primary Endpoint
marginal adaptation assessed by clinical evaluation using dental mirror and probe

Study Overview

Brief Summary

In teeth requiring laminate veneers with amelogenesis imperfecta Will application of galla chinensis before Bonding of laminate veneers with adhesive resin cement provide better survival rate than conventional Bonding method

Detailed Description

one year Clinical evaluation of laminate veneers with amelogenesis imperfecta Will application of galla chinensis before Bonding of laminate veneers with adhesive resin cement provide better survival rate than conventional Bonding method

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All subjects are required to be:
  • From 18-60 years old, and able to read and sign the informed consent document.
  • Physically and psychologically able to tolerate conventional restorative procedures
  • Have no active periodontal or pulpal diseases, have teeth with good restorations
  • Patients with teeth problems indicated for laminate veneer (e.g. discoloration, fracture not involve more than 50% enamel loss, mild malposition, ....)
  • Willing to return for follow-up examinations and evaluation

Exclusion Criteria

  • Patients in the growth stage with partially erupted teeth
  • Patient with fractured teeth of more than 50% enamel loss
  • Patients with poor oral hygiene and motivation
  • Pregnant women
  • Psychiatric problems or unrealistic expectations
  • Lack of opposite occluding dentition in the area intended for restoration

Outcomes

Primary Outcomes

marginal adaptation assessed by clinical evaluation using dental mirror and probe

Time Frame: 1 year

clinical evaluation of marginal adaptation

Secondary Outcomes

  • Patient satisfaction assessed using a Questionnaire(1 Year)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mohammed Gamal Fahmy Mohammed

B.D.S

Cairo University

Similar Trials