Actively Recruiting
Peri-Implant Soft Tissue Integration in Humans: Influence of Material
Led by Centre Hospitalier Universitaire de Liege · Updated on 2024-09-05
40
Participants Needed
1
Research Sites
53 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Peri-Implant Soft Tissue Integration in Humans: Influence of Material
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants must voluntarily sign the informed consent form before study procedures
- Patients aged 18 years or older
- Patients with one or more missing teeth in the upper (maxillary) or lower (mandible) jaw seeking implant therapy
- Male and female patients
- Patients in good systemic health classified as ASA I or II with no contraindications for oral surgery
- Patients requiring tooth replacement where the tooth was extracted or lost at least 12 weeks before implantation
- Presence of at least 3 mm of fibrous mucosa in the bucco-lingual dimension
- Full mouth plaque score (FMPI) of 25% or less
- Implant site must allow placement of an implant with at least 4 mm diameter
You will not qualify if you...
- Autoimmune diseases requiring medical treatment
- Medical conditions needing prolonged steroid use
- Use of intravenous bisphosphonates or oral bisphosphonates for more than 3 years
- Current local or systemic infections; patients with gingivitis or active infection must be treated before entering the study
- Current pregnancy or breastfeeding
- Alcoholism or chronic drug abuse
- Immunocompromised status
- Uncontrolled diabetes
- Smoking
- Prisoner status
- Implant diameter less than 4 mm (narrow implants)
- Any condition or circumstance that, in the investigator's opinion, would prevent study completion or interfere with data analysis, including history of non-compliance or unreliability
AI-Screening
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Trial Site Locations
Total: 1 location
1
Clémentine Canuel
Liège, Belgium, 4000
Actively Recruiting
Research Team
C
Clémentine Canuel, MsD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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