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Clinical Trials/NCT03252106
NCT03252106CompletedNot Applicable

Long-term Effectiveness of Contour Augmentation in Sites With Early Implant Placement

University of Bern2 sites in 1 country20 target enrollmentStarted: October 10, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
20
Locations
2
Primary Endpoint
Effectiveness of contour augmentation

Study Overview

Brief Summary

In this prospective case series study, 20 patients with an implant-borne single crown following early implant placement with simultaneous contour augmentation will be followed for 10 years. Clinical, radiologic, and esthetic parameters will be assessed. In addition, cone beam computed tomography (CBCT) will be used at 10 years to examine the facial bone wall and compared to the 6 year data.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
20 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Single tooth gaps post extraction in the esthetic zone
  • Written informed consent

Exclusion Criteria

  • Heavy smoking (more than 10 cigarettes per day)

Arms & Interventions

Contour augmentation

Experimental

Intervention: Contour augmentation with implant placement (Procedure)

Outcomes

Primary Outcomes

Effectiveness of contour augmentation

Time Frame: 10 year examination

Measurement of facial bone wall width with cone beam CTs (in mm)

Secondary Outcomes

  • Peri-implant bone loss over time(10 year examination)
  • Esthetic examination(10 year examination)
  • Peri-Implant soft tissue health(10 year examination)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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