NCT03252106CompletedNot Applicable
Long-term Effectiveness of Contour Augmentation in Sites With Early Implant Placement
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- University of Bern
- 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
Study Sites (2)
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