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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02937220
Other study ID # CEBD-CU-2016-10-223
Secondary ID
Status Not yet recruiting
Phase N/A
First received October 16, 2016
Last updated October 17, 2016
Start date December 2016
Est. completion date December 2017

Study information

Verified date October 2016
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority Egypt: Ministry of Higher Education
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the influence of superstructure material on crestal bone resorption and esthetic outcome of dental implants in patients with single missing tooth in the aesthetic zone.


Description:

The transfer of occlusal forces to the implant bone interface greatly influence the long term prognosis of implants and crestal bone resorption. Accordingly this study will investigate the influence of metal ceramic crowns and monolithic zirconia crowns on crestal bone resorption under loading. Also these crown materials greatly influence the final aesthetic outcome of the definitive restoration, which will be evaluated using the pink and white aesthetic scoring systems.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 34
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

1. Patients above 18 years old.

2. Patients able to read and sign the informed consent document. 3. Medically free patients or with controlled systemic disease.

4. Patients with good bone quality and quantity evaluated using C.B.C.T. 5. Patients willing to return for follow-up examinations and evaluation. 6. Patients having single missing recently extracted premolar tooth.

Exclusion Criteria:

1. Young patients in growth stage.

2. Patients with unsuitable implantation sites (patients with major boney defects or sever bone resorption)

3. Pregnant women to avoid any complication that may occur in dental office.

4. Patients with uncontrolled systemic disease (hypertensive patient or uncontrolled diabetic patient)

5. Psychiatric problems or unrealistic expectations.

6. Multiple adjacent missing teeth.

7. Patients with bad oral hygiene

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
monolithic zirconia crown
New crown material used as final restoration for dental implants
metal ceramic crown
Conventional crown material used as final restoration for dental implants

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary P.E.S. Pink aesthetic scoring system for soft tissue aesthetics 1 year No
Secondary crestal bone resorption 1 year No
See also
  Status Clinical Trial Phase
Not yet recruiting NCT05940662 - Cost Effectiveness of Various Implant Placement Protocols in the Esthetic Zone Phase 4