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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03214549
Other study ID # CairoUni
Secondary ID
Status Not yet recruiting
Phase N/A
First received July 3, 2017
Last updated July 9, 2017
Start date July 13, 2018
Est. completion date October 1, 2018

Study information

Verified date July 2017
Source Cairo University
Contact housham N Musa, master
Phone 00201068778033
Email dr_hishamnabeel@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate tooth sensitivity and marginal adaptation of porcelain laminates veneers prepared with modified gull wing preparation and conventional preparation.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 38
Est. completion date October 1, 2018
Est. primary completion date October 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Procedure:
gull wing preparation of laminates veneers
preparation involving mesial and distal extension further lingualy.
conventional preparation of laminates veneers
preparation not involving mesial and distal extension further lingualy.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary measuring marginal adaptation of laminates veneers using stero-microscope 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 measuring tooth sensitivity after tooth preparation for laminates veneers 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
Slight sensitivity
Moderate sensitivity
Severe pain
one week after tooth preparation
See also
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