Investigation of Biofilm Formation on Temporary push-on Rings of Implant Crowns
Recruiting
N/A
Interventional Study
Dental Plaque
Oral Biofilm
Peri-implantitis
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 33 (estimated)
- Sponsor
- University Hospital, Basel, Switzerland · Other
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About This Trial
This in-vivo study investigates early (48h), mature (2 weeks) and long-term (3 months) biofilm formation and composition on temporary push-on cones (exchangeable conical rings) made of noble-alloy-based materials (Pagalinor, PA) in comparison to Titanium-6Aluminum-7Niobium alloy (TAN) presently used in the transmucosal portion of dental implant abutments.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Informed Consent signed by the subject
* Presence of one or more bone level titanium implant prior to insertion of the final restoration
* No systemic illness
* No heavy smoking (smoking \<10 cigarettes/day)
* No pregnancy
* No active periodontitis (probing pocket depth ≤4 mm)…
Contacts