K08.2
Conditions
Interventions
Group 1: Bone augmentation of the jaw bone with autologous (patients own) bone
Group 2: Bone augmentation of the jaw bone with allogenic bone (human donor bone)
Sponsors
Universitätsmedizin der Johannes Gutenberg-Universität Mainz
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients who have reached the age of 18 and who receive bone augmentation of the jaw bone, either with an autologous bone block from the jaw angle or with an allogeneic, human bone block from a humanmdonor, at one of the two participating hospitals (Bundeswehrzentralkrankenhaus Koblenz, Universitätsmedizin Mainz) before a planned implant treatment are included. At the Bundeswehrzentralkrankenhaus Koblenz, both civilian patients and soldiers are included in the study. Both procedures are routinely used in the two participating hospitals as part of patient care.
Exclusion criteria
Exclusion criteria: Excluded from the study are patients who have not yet reached the age of 18, as well as patients who have received or have had bone augmentation of the jaw at another clinic outside of the two mentioned. Patients will only be asked if they wish to participate in the voluntary patient survey during subsequent follow-up.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Stress, pain, nerve damage, swelling, duration to freedom from symptoms, satisfaction. Since this is an observational study based on a questionnaire, both primary and secondary outcome measures are collected via the questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Comorbidity due to bone harvesting, preference and opinion donor bone. | — |
Countries
Germany
Contacts
Public ContactPeer W. Kämmerer
Klinik und Poliklinik für Mund-, Kiefer- und Gesichtschirurgie der Universitätsmedizin Mainz
Outcome results
None listed