Periodontitis Periimplantitis
Conditions
Interventions
Group 1: During routine clinical treatment, the following clinical parameters are recorded at 6 sites per tooth/implant (buccal and oral, mesial: mesio- buccal/ oral, distal): probing depths with blee
Sponsors
Philipps-Universitär Marburg/Lahn, Med. Zentrum für Zahn-, Mund- und Kieferheilkunde, Abteilung für Orofaziale Prothetik und Funktionslehre
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: Patients who have had prosthetic treatment with implants and fixed superstructures (crowns and bridges) for at least 3 years and who have regularly participated in the 3-6 month recall programme of the Department of Orofacial Prosthetics and Functional Sciences at the Medical Centre for Dental, Oral and Maxillofacial Medicine in Marburg.
Exclusion criteria
Exclusion criteria: Systemic diseases (e.g. cardiovascular diseases, diabetes, osteoporosis), untreated caries, pregnancy, current orthodontic treatment, abstinence from drugs and alcohol, regular medication, mental illness, smokers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The aim of the study is to demonstrate a possible correlation between soft tissue thickness and bone level at teeth and implants. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary endpoint of the study is to demonstrate a possible correlation between soft tissue thickness and probing depth on teeth and implants. | — |
Countries
Germany
Contacts
Public ContactReiner Mengel
Philipps-Universitär Marburg/Lahn, Med. Zentrum für Zahn-, Mund- und Kieferheilkunde, Abteilung für Orofaziale Prothetik und Funktionslehre
Outcome results
None listed