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Bilateral Condylar Fractures Registry

NCT02884765 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 227

Last updated 2024-07-16

No results posted yet for this study

Summary

Prospective data will be collected in approximately 250 patients sustaining BCFx with or without any additional fracture(s) of the symphysis. Patients will be followed according to the standard (routine) at approximately 6 weeks and 3 months after the treatment. Data collection will include fracture details (i.e. classification, mechanism of injury), treatment details, functional and patient-reported outcomes, and anticipated or procedure-related adverse events (i.e. complications).

Conditions

  • Bilateral Condylar Fracture of the Mandible

Interventions

PROCEDURE

Non-surgical

Non-surgical treatment in both condylar fractures

PROCEDURE

Non-surgical / Surgical

Non-surgical treatment in one condylar fracture and surgical treatment of the contralateral fracture

PROCEDURE

Surgical

Surgical treatment in both condylar fractures

Sponsors & Collaborators

  • AOCMF

    collaborator OTHER

  • AO Clinical Investigation and Publishing Documentation

    lead OTHER

Principal Investigators

  • Edward Ellis 3rd, DDS MS · University of Texas

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-31
Primary Completion
2023-03-31
Completion
2023-12-31

Countries

  • United States
  • Finland
  • Germany
  • Malaysia
  • Mexico
  • Netherlands
  • Pakistan
  • Slovenia
  • South Africa
  • Spain
  • Switzerland
  • Taiwan
  • Ukraine
  • Uruguay

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02884765 on ClinicalTrials.gov