Visual Prognosis in Non-Penetrating Corneal Blast Injuries
Completed
Conditions studied: Corneal Foreign Body Following Blast Injury
In brief
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.
Key facts
- Study ID
- NCT00414219
- Run by
- Walter Reed Army Medical Center
- People needed
- 40
- Starts
- 2004-11-01
- Expected to finish
- 2007-05-01
- Last updated by the study team
- 2010-12-30
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- 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
You may not qualify if…
- 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.
Where it is running
- Walter Reed Army Medical Center — Washington D.C., District of Columbia, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.