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A Prospective Analysis On The Clinical Utility Of 3d Printing Manufacturing Patient-Specific Guide With Orbital Fracture

Not Applicable
Recruiting
Conditions
Injury, poisoning and certain other consequences of external causes
Registration Number
KCT0008835
Lead Sponsor
Konkuk University Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
448
Inclusion Criteria

a) Adult men and women between the ages of 19 and 69
b) Patients with pure orbital fractures scheduled for orbital fracture repair
c) A research subject who fully understands the consent statement and consents in writing

Exclusion Criteria

a) Cases where orbital fracture reduction was not performed in patients with two or more fractures
b) Acute severe sinusitis (acute fulminant sinusitis)
C) Those who are judged inappropriate to participate in this clinical trial according to the judgment of the researcher

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in orbital volume in the defective area compared to the normal orbit after surgery (6 months after surgery, however, in the case of patients whose last visit was 3 months due to no complications, it is replaced with 3-month CT)
Secondary Outcome Measures
NameTimeMethod
umber of complications;Changes in orbital and defect volume;operation time;best corrected vision;Surgeon's Satisfaction
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