Clinical Trials Directory

Trials / Completed

CompletedNCT00129077

Does the Use of a Moisture Chamber Decrease the Incidence of Corneal Abrasions in Critically Ill Pediatric Patients?

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
207 (actual)
Sponsor
Ann & Robert H Lurie Children's Hospital of Chicago · Academic / Other
Sex
All
Age
2 Weeks – 17 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to identify the incidence of scratches on the surface of the eye in children who cannot blink due to medication use and to identify how best to reduce the risk of a scratch on the surface of the eye when patients are using specific medicines.

Detailed description

Critically ill children may require neuromuscular blockade as a treatment modality. These children require careful eye care to prevent corneal abrasions. However, current evidence does not exist to guide best practices on eye care. This research study will evaluate 2 types of eye care therapy. The eyes will be randomly assigned to the control or experimental eye care therapy group. The control eye will receive lubricating ointment every 6 hours. The experimental eye will receive lubricating ointment every 6 hours and have a plastic covering to create a moisture chamber. Using daily fluorescein staining to detect corneal abrasions, each child will be studied for up to 9 days. Children who develop corneal abrasions will be discharged from the study and the primary care team will be notified. The two groups will then be compared to determine the therapy associated with the lowest incidence of corneal abrasions.

Conditions

Interventions

TypeNameDescription
PROCEDUREplastic wrap over eye & lubrication applied q6 hrs

Timeline

Start date
2004-03-01
Completion
2006-12-01
First posted
2005-08-11
Last updated
2007-07-10

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00129077. Inclusion in this directory is not an endorsement.