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Visual Prognosis in Non-Penetrating Corneal Blast Injuries
This study is ongoing, but not recruiting participants.
Study NCT00414219   Information provided by Walter Reed Army Medical Center
First Received: December 20, 2006   Last Updated: November 9, 2007   History of Changes

December 20, 2006
November 9, 2007
November 2004
 
 
 
Complete list of historical versions of study NCT00414219 on ClinicalTrials.gov Archive Site
 
 
 
Visual Prognosis in Non-Penetrating Corneal Blast Injuries
Visual Prognosis in Non-Penetrating Corneal Blast Injuries

The purpose of this study is to assess visual quality of patients with non-penetrating, non-metallic, stable corneal foreign bodies. Visual quality will be assessed by examining visual acuity, wavefront analysis and contrast sensitivity. Drawings, photographs, and confocal microscopy will be used to document clinical examination of the cornea at baseline and on follow-up examinations.

 
 
Observational
Cohort, Prospective
Corneal Foreign Body Following Blast Injury
Behavioral: Visual quality of patients with corneal eye injuries
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Active, not recruiting
40
May 2007
 

Inclusion Criteria:

  • Informed consent
  • Access to medical care at Walter Reed Army Medical Center
  • Age 18 years or older
  • Corneal foreign bodies from blast injuries
  • Available for evaluation at Walter Reed

Exclusion Criteria:

  • Residual, recurrent or active ocular disease in the designated eye as determined by exam and history.
  • Penetrating ocular trauma or injury to the posterior segment
  • Prior history of ocular surgery
  • Any physical or mental impairment that would preclude participation in any of the examinations.
  • Any ocular abnormality other than corneal foreign bodies that have any impact on vision (i.e. other abnormalities from trauma such as retinal detachment, corneal laceration, traumatic cataract, or abnormalities unrelated to trauma such as herpes.
Both
18 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00414219
 
WRAMC WU# 04-23010
Walter Reed Army Medical Center
 
Principal Investigator: Dain Brooks, MD Ophthalmology Service, Walter Reed Army Medical Center
Walter Reed Army Medical Center
November 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP