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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02711436
Other study ID # HYMC-0022-16
Secondary ID
Status Not yet recruiting
Phase N/A
First received March 14, 2016
Last updated March 14, 2016
Start date April 2016
Est. completion date April 2017

Study information

Verified date March 2016
Source Hillel Yaffe Medical Center
Contact Yuval Cohen, MD, PhD
Email dr.yuvalcohen@gmail.com
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

The aim of the study is to compare orbital and central nervous system (CNS) imaging with Computed Tomography (CT) scan to that of Fast Magnetic Resonance Imaging (Fast MRI) in children with mild, moderate or severe orbital cellulitis with medical indications for imaging.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date April 2017
Est. primary completion date April 2017
Accepts healthy volunteers No
Gender Both
Age group 6 Months to 20 Years
Eligibility Inclusion Criteria:

- Children with orbital cellulitis with indications for imaging

Exclusion Criteria:

- All others

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Device:
Computed Tomography Scan

Fast Magnetic Resonance Imaging


Locations

Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (1)

Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary MRI sensitivity for the detection of orbital cellulitis compared to CT MRI results will be compared to CT results One year No
See also
  Status Clinical Trial Phase
Withdrawn NCT01504568 - The Use of Prophylactic Antibiotics in Isolated Blowout Fractures N/A