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Clinical Trials/NCT03333889
NCT03333889
Unknown
Not Applicable

Patient Satisfaction and Crestal Bone Loss of Polymer Infiltrated Ceramic Network Versus Lithium Disilicate Implant Hybrid Abutment Crowns in Esthetic Zone

Cairo University1 site in 1 country36 target enrollmentJanuary 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hybrid Crowns on Single Implants in Esthetic Zone
Sponsor
Cairo University
Enrollment
36
Locations
1
Primary Endpoint
patient satisfaction
Last Updated
8 years ago

Overview

Brief Summary

P: Population: Patients requiring single unit implant restoration in esthetic zone I: Intervention: Polymer-infiltrated-ceramic-network abutment crown (VITA Enamic-VITA Zahnfabrik) C: Comparison: Lithium disilicate ceramic abutment crown (IPS e. max-Ivoclar Vivadent) O: Outcome: patient satisfaction , crestal bone loss and periodontal parameters T: Time: 12 months S :Randomized controlled trial research question:For patients receiving implants in esthetic zone, Does the use of polymer-infiltrated-ceramic-network hybrid abutment crown offer better patient satisfaction , less bone loss and better peri-implant clinical parameters when compared to lithium disilicate hybrid abutment crowns?

Registry
clinicaltrials.gov
Start Date
January 2018
End Date
April 2019
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Inas Adel Mahmoud

assistant lecturer,fixed prosthodontic department, faculty of oral and dental medicine

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Patients above 18 years old.
  • Patients able to read and sign the informed consent document.
  • Medically free patients or with controlled systemic disease.
  • Patients with good bone quality and quantity evaluated using C.B.C.T.
  • Patients willing to return for follow-up examinations and evaluation.
  • Patients having single missing recently extracted premolar tooth.

Exclusion Criteria

  • Young patients in growth stage.
  • Patients with unsuitable implantation sites (patients with major boney defects or sever bone resorption)
  • Pregnant women to avoid any complication that may occur in dental office.
  • Patients with uncontrolled systemic disease (hypertensive patient or uncontrolled diabetic patient)
  • Psychiatric problems or unrealistic expectations.
  • Multiple adjacent missing teeth.
  • Patients with bad oral hygiene. -

Outcomes

Primary Outcomes

patient satisfaction

Time Frame: 12 months

using visual analogue scale (o-unsatisfied up to max 10 satisfied)

Secondary Outcomes

  • crestal bone loss(12 months)

Study Sites (1)

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