Full-Contour Monolithic Zirconia Full-Mouth Implants: Post-Insertion Outcomes

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational cohort tracks prosthodontic and biological complications after implant-supported full-mouth rehabilitations made from full-contour monolithic zirconia, without buccal veneers. Investigators calibrate assessments for complication types and aim for high inter-observer agreement. Data are collected from a private clinic in Lisbon, focusing on patients with at least one year of function. No magnification tools are used during evaluation, and the study follows patients receiving maxillary and/or mandibular full-mouth FC-MZ restorations.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Maxilla and/or Mandible Implant full-mouth restoration
* Full-contour monolithic zirconia restoration (without ceramic veneer)
* be at least 18 years of age;
* present no systemic or local absolute contraindications for endosseous implant placement;
* at least 1 Year Follow-up

Exclusion Criteria:

* the presence of any systemic disease or condition that could compromise postoperative healing or osseointegration.
* Not full mouth rehabilitation
* Rehabilitations with ceramic veneers (buccal veneer or feldspathic veneered zirconia)

Where it's running

• Instituto de Implantologia
  Lisbon, Lisbon District, Portugal Recruiting

Study contacts

• Principal investigator: Artur Simões, Msc — Implantology Institute
• Study coordinator: Artur Simões, Msc
• Email: artursimoes@institutoimplantologia.com
• Phone: 217210980

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• How full-arch dental implants affect oral health quality of life

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.