Interest of Bone Substitute Material in Immediate Complete Denture (PANORAMIX)
Alveolar Bone Loss, Denture Complete Immediate, Bone Substitute
About this trial
This is an interventional treatment trial for Alveolar Bone Loss focused on measuring Immediate complete denture, Alveolar ridge resorption, Alveolar bone loss, Bone substitute material, Edentulism
Eligibility Criteria
Inclusion Criteria:
- Candidates for maxillary immediate complete denture, presenting a Kennedy
- Class I partial dentition (bilateral posterior tooth loss)
- Over 18 years of age
- Healthy adhering gingiva
- Willing to participate in the study, able to sign the consent form
Exclusion Criteria:
- Medical conditions contraindicating oral surgery: progressive cancer history of radiotherapy in the head and neck region major neurological disease anti-coagulant treatment with prothrombin time<30% valvulopathy, hematologic disease, agranulocytosis, serious heart failure, recent myocardial infarction < 5 years immune deficiency, AIDES osteomalacia hepatic or renal insufficiency unregulated diabetes long-term steroids treatment bisphosphonates
- Allergy to collagen
- Pregnant or nursing women
- Persons specially protected
- Non-affiliated with the social security system persons
Sites / Locations
- Henri Mondor Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Bone substitute material group
Conventional protocol
Immediate denture placement following extractions and alveolar sockets filling with bone substitute material
Immediate denture placement following the conventional protocol