About this trial
This study will evaluate the behavior of the implant-supported restorations (prosthesis) placed into the areas grafted with the 3D printed customized bone (personalized graft produced to fit a specific bone defect), as well as the volume contraction of the printed bone.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Systemically healthy individuals
over 18 years of age
Subjects that received regenerative surgical treatment by customized 3D printed blocks.
Subjects must agree to participate in the study and agree to sign the Informed Consent.
Disqualifiers
Subjects with ilness that avoid their presence to the clinical evaluation
ISubjects who have lost the customized blocks
Subjects who do not agree to participate in the study will be excluded.
Trial population
This prospective cohort study will evaluate the peri-implant conditions of patients who received regenerative procedures using 3D-printed blocks at the UnG Clinic. To this end, participants will be selected from the UnG graduate clinic who received the regenerative treatment using 3D-printed blocks between 2019 and 2025. Participants selected for the study must sign the Informed Consent Form (ICF) after a verbal and written explanation of the project. Subjects will receive oral hygiene instruction and professional prophylaxis prior to clinical examinations.
Trial design
Cohort
Prospective
Treatments tested in this trial
Clinical evaluation
Other interventionClinical parmeters and radiographical analysis
Treatment groups
Trial outcomes
Primary outcomes
Periodontal Clinical Parameter of the implants Placed in the Grafted area
Marginal Bone Loss \< 2mm
Secondary outcomes
Bone Graft Volume Alteration
Tomographic Volumetric Measurement (mm3) of the 3D printed graft after a period ranged between 1 to 6 years
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: