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
| Type | Name | Description |
|---|---|---|
| OTHER | Mucointegration | Placement 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.