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Passive Fit of Implant-Supported Complete-Arch Prostheses Using Digital Workflows

RecruitingNAAges 18 Years - anyAllUniversidad Complutense de Madrid
NCT07315620 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The goal of this clinical trial is to evaluate and compare three digital workflows for the fabrication of definitive implant-supported full-arch prostheses in adult patients requiring fixed implant rehabilitation. The main questions it aims to answer are: * Does an automated AI-assisted digital workflow improve the passive fit of definitive full-arch implant-supported prostheses compared with manual and splint-guided alignment workflows? * Are there differences in marginal, geometric, mechanical, and radiographic passivity among the three digital workflows? Researchers will compare manual CBCT-STL alignment, splint-guided alignment, and automated AI-assisted CBCT-STL alignment to see if the degree of digital workflow automation affects the passive fit of definitive full-arch implant-supported prostheses. Participants will: * Be adults (18 years and older) indicated for fixed implant-

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📋 Eligibility rules (as published)
Inclusion Criteria: 1. Adults aged 18 years or older. 2. Patients indicated for fixed implant-supported full-arch rehabilitation in the maxilla or mandible. 3. Presence of clinically stable, osteointegrated titanium implants suitable for prosthetic rehabilitation. 4. Absence of clinical or radiographic signs of peri-implant disease. 5. Ability to understand the study procedures and provide written informed consent. 6. Willingness and ability to attend all required clinical visits and evaluations. Exclusion Criteria: 1. Presence of peri-implant mucositis or peri-implantitis at the time of evaluation. 2. Implant mobility or implant positioning that prevents proper prosthetic rehabilitation. 3. Uncontrolled systemic medical conditions that could interfere with study participation or prosthetic treatment. 4. Cognitive, psychological, or medical conditions that limit the ability to comply with study procedures. 5. Inability to complete the required clinical evaluations or follow the study protocol, as judged by the investigator.
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What it tests

  • CBCT-STL Alignment Workflow
  • Splint-Guided Alignment Workflow
  • Automated AI-Assisted CBCT-STL Alignment Workflow
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Where

1 site
University Complutense of Madrid
Madrid, Spain
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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