E. Max Laminate Veneers With and Without Using Galla Chinnesis as Natural Cross Linking and Remineralizing Agent

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

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02994862

Enrollment

Registered

2016-12-16

Start date

2016-12-31

Completion date

2017-12-31

Last updated

2016-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Amelogenesis Imperfecta

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

Interventions

OTHERGalla Chinnesis

new Remineralizing Agent before Bonding to teeth with amelogenesis imperfecta

OTHERConventional Bonding

Normal Bonding Protocol

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender

ALL

Age

18 Years to 60 Years

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame	Description
marginal adaptation assessed by clinical evaluation using dental mirror and probe	1 year	clinical evaluation of marginal adaptation

Secondary

Measure	Time frame	Description
Patient satisfaction assessed using a Questionnaire	1 Year	Questionnaire for patient satisfaction

Contacts

Primary ContactMohammed mohammed, B.D.S

mgamal400@gmail.com01226500339

Backup ContactJylan Elguindy, Phd

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026