- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03214549
Comparison in Marginal Adaptation Between Conventional and Gull Wing Preparation in Laminates Veneers
Marginal Adaptation of E.Max Laminate Veneers Prepared With Modified Gull Wing Preparation and Conventional Preparation
Study Overview
Status
Conditions
Detailed Description
Visit 1: Preoperative records, face-to-face adherence reminder session, clinical, radio-graphic examination and primary impression for diagnostic cast construction.
Visit 2: Teeth preparation, secondary impression,temporary restoration and teeth sensitivity evaluation using United States Public Health Service criteria.
Visit 3: Placement and permanent cementation of the final restoration
Visit 4: marginal adaptation measurement by electron microscope using impression replica.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: housham N Musa, master
- Phone Number: 00201068778033
- Email: dr_hishamnabeel@hotmail.com
Study Contact Backup
- Name: rayan R dahab, master
- Phone Number: 00201068775688
- Email: rayanrabiedahab@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- From 18-40 years old, be able to read and sign the informed consent document.
- Be 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.
- Be 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.
- Patient with post and core endodontically treated teeth.
- Psychiatric problems or unrealistic expectations.
- Lack of opposite occluding dentition in the area intended for restoration
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: gull wing preparation veneers
intervention: gull wing preparation in laminates veneers proximal margin of the preparation is placed toward the lingual .The area of the proximal margin between the contact area and the gingival papilla is placed even further to the lingual.
This preparation design helps to hide the margin when the restorations are viewed from an angle.
|
preparation involving mesial and distal extension further lingualy.
Other Names:
|
Active Comparator: conventional preparation veneers
intervention: conventional preparation in laminates veneers preparation of veneers without lingual extension of preparation in mesial and distal areas
|
preparation not involving mesial and distal extension further lingualy.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
measuring marginal adaptation of laminates veneers using stero-microscope
Time Frame: immediately before laminates delivery up to 4 week sfter tooth preparation
|
marginal adaptation of laminates veneers will be assess as follows, before laminates cementation, an impression material will be placed in the fitting surface of the veneers and placed over the reduced tooth using finger pressure, after material set the impression replica is separated from the laminates and the replica is section and measures under stero-microscope for marginal adaptation, measurement will be performed in eight different points on the buccal and mesio-distal sections, measurement will be in micrometer.
|
immediately before laminates delivery up to 4 week sfter tooth preparation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
measuring tooth sensitivity after tooth preparation for laminates veneers
Time Frame: one week after tooth preparation
|
measurment will be acording tomodified United States Public Health Service (USPHS) criteria used for the clinical evaluations of the restorations. post-operative sensitivity 0 No symptoms
|
one week after tooth preparation
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CairoUni
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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