Clinical Trials Directory

Trials / Completed

CompletedNCT02117323

Corneal Opacities in Children

Observational Study on Corneal Opacities in Children

Status
Completed
Phase
Study type
Observational
Enrollment
54 (actual)
Sponsor
Oregon Health and Science University · Academic / Other
Sex
All
Age
1 Month – 18 Years
Healthy volunteers
Not accepted

Summary

A prospective observational study on corneal opacities in infants and children (1 month to 18 years old) will be conducted at CHLA. Most of these cases will be due to congenital corneal opacity (e.g. Peter's anomaly, mucopolysacharidoses) or scarring due to infectious keratitis. Sixty (60) subjects will be recruited. The children will be examined under anesthesia with a portable slit-lamp and OCT. An iVue OCT system (Optovue) attached to an operating microscope-style mount at CHLA will be used for the intraoperative scans. Both cross-sectional and 3-D OCT scans will be performed to assess opacity depth, pachymetry map, endothelial defects, and any abnormal adhesion between the cornea, iris and lens. The anterior chamber angle will also be imaged with cross-sectional OCT to assess angle depth, trabecular meshwork, Schwalbe's line, and possible peripheral iridocorneal adhesion or posterior embryotoxon. OCT of the crystalline lens will be obtained to assess the presence of cataract. Slit-lamp photography will be obtained, and gonioscopy will be performed if indicated. Corneal diameter will be measured with a caliper, and intraocular pressure will be measured with a tonopen (Reichert).

Conditions

Timeline

Start date
2011-09-01
Primary completion
2016-08-31
Completion
2016-08-31
First posted
2014-04-17
Last updated
2018-04-17

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02117323. Inclusion in this directory is not an endorsement.