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Clinical Trial Summary

- Baseline: - Standard preparation of the osteotomy - Placement of 2 dental implants - On each implant one of both types of healing abutments is placed - Suturing - Standardized radiography to measure bone-levels at baseline - Digital impression of the surrounding gingiva with an intra-oral scanner (a non-invasive method) to measure the baseline level of the gingiva - 2 weeks after Baseline: o Removal of the sutures - 4 weeks after Baseline: - A 2nd digital impression of the soft tissue with an intra-oral scanner - Collecting crevicular fluid by placing paperpoints in the provided apertures in the healing abutments for 60 seconds without bleeding. - Measuring of the pocket depth in the provided apertures in the healing abutments with an automated probe. - Removal of the Healing Abutment with the attached soft tissue en-bloque. - Placement of a new, regular, Encode Healing Abutment. - 10 weeks after Baseline: - Start of standard prosthetic procedure. In this study we expect that the soft tissue attachment (i.e. the gingival attachment) will be stronger and earlier achieved at the nano-structured healing abutments than at the normal, uncoated healing abutments. This would lead to a more stable soft tissue complex on the long rung and thus providing a more predictable aesthetic outcome. Secondly, a stronger attachment would mean a stronger barrier against micro-organisms and might influence the occurrence of peri-implantitis.


Clinical Trial Description

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NCT number NCT01620918
Study type Interventional
Source University Ghent
Contact
Status Completed
Phase N/A
Start date August 2012
Completion date August 2015