Comparison of patient satisfaction with the use of allogeneic bone blocks versus autologous bone blocks in alveolar ridge augmentation.

• Conditions: K08.2; Atrophy of edentulous alveolar ridge

• Registration Number: DRKS00027341
• Lead Sponsor: niversitätsmedizin der Johannes Gutenberg-Universität Mainz

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-12-07
• Study Completion: 2022-09-01
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 36

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

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.

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Stress, pain, nerve damage, swelling, duration to freedom from symptoms, satisfaction.<br><br>Since this is an observational study based on a questionnaire, both primary and secondary outcome measures are collected via the questionnaire.

Secondary Outcome Measures

Name	Time	Method
Comorbidity due to bone harvesting, preference and opinion donor bone.