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Device

3D digital scanning for maxillofacial prosthetics for Maxillofacial Abnormalities

N/A
Waitlist Available
Led By Kyle Vankoevering, MD
Research Sponsored by University of Michigan
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 6 months
Awards & highlights

Study Summary

This trial will use a 3D scanner to print a model of a prosthesis for each patient. The goal is to provide a new, faster method that preserves quality while reducing time for patients and providers.

Eligible Conditions
  • Maxillofacial Abnormalities
  • Craniofacial Dysmorphism
  • Prosthetic Treatment

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 6 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Number of hours spent to create the prosthetic
Number or weeks to create the final prosthesis
Time the participants spend in the clinic
Secondary outcome measures
Number of adverse events related to the prosthetic
Quality of life measures by modified Toronto Outcome Measure of Craniofacial Prosthetics (TOMCP) for extraoral prosthesis.
Prosthesis
+2 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: 3D digital scanning for maxillofacial prostheticsExperimental Treatment1 Intervention

Find a Location

Who is running the clinical trial?

University of MichiganLead Sponsor
1,810 Previous Clinical Trials
6,385,075 Total Patients Enrolled
Kyle Vankoevering, MDPrincipal InvestigatorUniversity of Michigan
David Zopf, MDPrincipal Investigator - University of Michigan
University of Michigan Hospital, Von Voigtlander Women's Hospital
1 Previous Clinical Trials
40 Total Patients Enrolled
~5 spots leftby Jun 2025
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