Phase
Condition
Lung Cancer
Musculoskeletal Diseases
Bone Diseases
Treatment
Surgical Resection and Reconstruction
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
The study includes patients with an initial pathological/histologic diagnosis ofmandibular involvement by oral tumors (such as OSCC, osteosarcoma, andameloblastoma), bisphosphonate- or immunomodulatory drug-induced osteonecrosis, andmandibular lesions from metastatic conditions originating from other sites includinglung, breast, prostate, or kidney.
Age 18 years and older
Bisphosphonate related osteonecrosis of the mandible
Immunomodulatory drugs induced mandibular osteonecrosis
Patients presented with ameloblastoma affecting the mandible
Patients presented with osteosarcomas of the mandible
Patients presented with oral metastases related mandibular lesions that areindicated for segmental resection, common primary tumor sites include lung, breast,prostate and kidney
Undergoing primary curative treatment with segmental resection of the mandible ≥2 cm
Intention to undergo mandibular reconstruction with autologous bone using a primary (one-stage) or secondary (two-stage) approach
Informed consent obtained, ie:
Ability to understand the content of the patient information/ICF
Willingness and ability to participate in the clinical investigation accordingto the registry plan (RP) o Signed and dated IRB/EC approved ICF OR
Written consent provided according to the IRB/EC defined and approvedprocedures for patients who are not able to provide to provide independentwritten informed consent
Exclusion
Exclusion Criteria:
Tumors affecting the condyle
Patients under palliative care
Previous extensive mandibular surgeries (including reconstructions, e.g., TMJreplacement) that may potentially confound the outcome measures
Intraoperative exclusion criteria:
Nonsegmental mandibular defect (eg. box resection/partial resection)
Segmental mandibular defect of less than 2 cm
Mandibular defects extending beyond the sigmoid notch into the condyles
Additional exclusion criterion:
• No osseous reconstruction with autologous bone performed within 18 months from resection
Study Design
Study Description
Connect with a study center
Medical University of Graz
Graz, 8036
AustriaSite Not Available
Universitätsklinikum Tübingen
Tübingen, Baden-Württemberg 72076
GermanyActive - Recruiting
University Hospital RWTH Aachen
Aachen, 52074
GermanyActive - Recruiting
University Hospital Charité
Berlin, 13353
GermanyActive - Recruiting
Hannover Medical School
Hannover, 30625
GermanyActive - Recruiting
Universitätsklinikum Heidelberg
Heidelberg, 69120
GermanyActive - Recruiting
University Hospital Leipzig
Leipzig, 04103
GermanyActive - Recruiting
Klinikum der LMU München
Munich, 80337
GermanyActive - Recruiting
Erasmus University Medical Centre
Rotterdam, 3015 GD
NetherlandsActive - Recruiting
National Medical and Surgical Center
Moscow, 125284
Russian FederationSite Not Available
12 de Octubre
Madrid, 28041
SpainActive - Recruiting
Uppsala University Hospital
Uppsala, 75185
SwedenActive - Recruiting
University Hospital Basel
Basel, 4031
SwitzerlandActive - Recruiting
University of California
Sacramento, California 95817
United StatesSite Not Available
University of Florida College of Medicine
Jacksonville, Florida 32209
United StatesActive - Recruiting
University of Illinois Chicago
Chicago, Illinois 60612
United StatesActive - Recruiting
Mount Sinai Hospital
New York, New York 10029
United StatesActive - Recruiting
John Peter Smith Health Network
Fort Worth, Texas 76104
United StatesActive - Recruiting
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