Screening for Research Subjects With Anterior Segment Diseases
NCT ID: NCT00088348
Last Updated: 2017-07-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
600 participants
OBSERVATIONAL
2004-07-13
2008-08-20
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Patients of any age with anterior segment disease may be eligible for this screening study. Participants will be evaluated with some or all of the following tests and procedures, depending on the nature of their eye problem:
* Medical history and brief physical examination.
* Eye examination, including measurement of visual acuity (eye chart) and eye pressure, examination of the pupils, eye movements, structures in the front of the eye (cornea, conjunctive, etc.), the lens, and the structures in the back of the eye (retinal, optic nerve, etc.).
* Photographs of the eye to help assess the status of the cornea and conjunctive and to evaluate any changes that may occur in the future.
* Assessment of tear and surface status. The amount of tears the eyes can produce is measured by placing a small piece of sterile paper in the corner of the eye every 5 minutes. Special orange and green dyes are placed in the eyes to determine the health status of the surface of the eye.
* Corneal or conjunctival biopsy. A small tissue sample from the surface of the eye may be removed for laboratory examination to help diagnose a condition that is unclear. For this procedure, the eye is numbed with anesthetic eye drops. The required tissue is collected, an antibiotic ointment is placed in the eye to prevent infection, and a patch may be placed over the eye for 12 to 24 hours.
* Blood draw for tests to study the cause of the patient's eye disease.
* Other diagnostic tests as needed.
* DNA testing to look for a genetic pattern associated with the patient's eye disease.
Patients who are found eligible for an NEI study will be offered participation in that study. Patients who are not eligible for current studies will be advised about treatment options.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Screening for NEI Clinical Studies
NCT00001734
Evaluation and Treatment of Patients With Inflammatory Eye Diseases
NCT00006188
Immune Responses to Antigens in Non-infectious Eye Inflammatory Diseases
NCT00357071
The Vitreous Proteome and Inflammatory Mediators in Ocular Inflammatory Disease
NCT00331331
Analysis of Eye Tissue
NCT00001224
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
To participate in this screening study, a patient must have a history of anterior segment disease. Patients of all ages are eligible.
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Eye Institute (NEI)
NIH
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, United States
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Holland EJ. Epithelial transplantation for the management of severe ocular surface disease. Trans Am Ophthalmol Soc. 1996;94:677-743.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
04-EI-0241
Identifier Type: -
Identifier Source: secondary_id
040241
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.