Skip to main content
Clinical Trials/NL-OMON40820
NL-OMON40820
Completed
Not Applicable

Single final vs. multiple temporary implant abutments: A prospective randomized controlled clinical trial of peri-implant hard/soft tissue and bacteriological changes - Single or multiple abutments

Academisch Centrum Tandheelkunde Amsterdam0 sites40 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healed extraction site
Sponsor
Academisch Centrum Tandheelkunde Amsterdam
Enrollment
40
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Patients of at least 25 years of age and who are able to sign an informed consent.
  • 2\. In need of a single implant.
  • 3\. Healed site (healed site defined by restored gingiva, free of inflammation and scar tissue (Zuhr, Hurzeler 2012\. Book), with a keratinized band of 3mm from crest to muco\-gingival junction, and sufficient osseous architecture to receive an implant (Koutouzis 2013\) with a minimal diameter of 3\.5 mm).
  • 4\. (Pre)molar region.
  • 5\. At least one neighbouring tooth is present.
  • 6\. Absence of visible active periapical or periodontal inflammation.
  • 7\. Adequate oral hygiene: PI\< 20%, BoP\< 20%.
  • 8\. Sufficient occlussal units mesial or distal and antagonizing, including the diastema to
  • be restored: 4 occlusal units.

Exclusion Criteria

  • 1\. Medical condition that contraindicates surgery: ASA \-score \>\= III
  • 2\. History of radiotherapy in the head and neck region.
  • 3\. History of Biphosphonate medication.
  • 4\. Medium smokers \>\= 10 cigarettes per day.
  • 5\. Patients unwilling or incapable of signing the informed consent.
  • 6\. Active caries

Outcomes

Primary Outcomes

Not specified

Similar Trials