K08.1
Conditions
Interventions
Group 1: Patients with immediate implant insertion and immediate restoration in region 15 -25 in the upper jaw
Measurements at 6 sites per implant
• pocket probing depth (PD):
• Bleeding on probing (B
Sponsors
Goethe Universität Frankfurt, Zentrum der Zahn-, Mund- und Kieferheilkunde (Carolinum), Zahnärztliches Universitäts-Institut gGmbH, Poliklinik für Zahnärztliche Chirurgie und Implantologie
Eligibility
Sex/Gender
All
Age
18 Years to 69 Years
Inclusion criteria
Inclusion criteria: - Males and females with an age of 18 to 69 years - Planned single tooth replacement in maxilla (15-25 FDI) allowing the placement of a single implant - Subject shall have a stable occlusal relationship - Patient has been informed of the follow-up visits and is willing to return to the clinical center for these follow-up visits - Subjects must have voluntarily signed the informed consent form before any study related action
Exclusion criteria
Exclusion criteria: - Systemic disease that would interfere with dental implant therapy (e.g. uncontrolled diabetes, osteoporosis) - Bone metabolism disorders or medication (steroids, bisphosphonate) -Pregnant or breastfeeding women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Health of periimplant tissue measured as: - Bleeding on probing (BOP) - Mucosal recession (MR) - probing depth (PD) - Clinical attachment level (CAL)) - Volume changes of the periimplant soft tissue Follow-up times: final prosthetic restoration, 6, 12 and 24 months after the final prosthetic restoration. | — |
Secondary
| Measure | Time frame |
|---|---|
| impact of the treatment protocol on the periimplant soft and hart tissue | — |
Countries
Germany
Contacts
Public ContactElisabeth Ferreira Schrenk
Zentrum der Zahn-, Mund- und Kieferheilkunde (Carolinum) der Goethe Universität Frankfurt, Zahnärztliches Universitäts-Institut gGmbH, Poliklinik für Zahnärztliche Chirurgie und Implantologie
Outcome results
None listed