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Clinical Trial Summary

Objective of the present study was to assess the peri-implant soft tissue profiles between argon plasma pre-treated (PT) and non-treated (NPT) abutments by comparing clinical and histological parameters 2 months after abutment placement.


Clinical Trial Description

Patients that need implant supported restoration were recruited for this study. At baseline a specific abutment was screwed at 20 N.Two months following healing abutment placement clinical measurements were evaluated. Endopoints of the study: Histological outcomes at 2 using traditional histological staining (ematossilin/eosin) Immunohistological outcomes at 2 using different stainings. Postoperative complications. Comparison between the histological outcomes and the preoperative clinical evaluation of the sites ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05821673
Study type Interventional
Source Studio Odontoiatrico Associato Dr. P. Cicchese e L. Canullo
Contact
Status Completed
Phase N/A
Start date June 21, 2021
Completion date June 30, 2022

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