Menu
Not yet recruiting NCT07405918

3D Printed Customized Bone Graft for Alveolar Regeneration: Longitudinal Cohort Evaluation

— Observational Periodontal Diseases Periodontal Bone Loss

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Clinical evaluation.
Who it may be relevant to
Registry conditions: Periodontal Diseases, Periodontal Bone Loss. Basic parameters: from 15 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

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.

Interventions

  • Other Clinical evaluation
    Clinical parmeters and radiographical analysis

Primary outcome measures

  • Periodontal Clinical Parameter of the implants Placed in the Grafted area [Time frame: 5 years]
Secondary outcome measures (1)
  • Bone Graft Volume Alteration [Time frame: 6 years]

Eligibility criteria

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07405918 · Guaruhos University

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗