Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05805033

Peri-Implant Soft Tissue Integration in Humans: Influence of Material

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Centre Hospitalier Universitaire de Liege · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to compare the mucointegration of 2 types of surface roughness of zirconia abutments with titanium. The surface roughness will be machined and ultra-polished.

Detailed description

After being informed about the study and potential risks, all participants give written informed consent and eligibility for study entry. The day of the surgery, patients will be randomized in machined zirconia or ultra-polished zirconia. After 8 weeks of healing, biopsy are separated in two groups according to the removal: * if the abutment come together with the surrounding soft tissues, it goes for a non decalcified histology for histometric measurements to determine the dimensions of biological width (sulcus depth, epithelial and connective adhesion) * if the abutment come separate of the surrounding tissue, the soft tissue goes for immunohistochemistry to analyse pro-inflammatory cells and vascularisation and the abutment for SEM analysis to calculate the percentage of adhesion of the cells on the abutment

Conditions

Interventions

TypeNameDescription
OTHERMucointegrationPlacement of abutment on a dental implant to study mucointegration

Timeline

Start date
2023-09-22
Primary completion
2024-06-18
Completion
2024-10-01
First posted
2023-04-07
Last updated
2024-09-05

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT05805033. Inclusion in this directory is not an endorsement.