NIH Clinical Research Studies

Protocol Number: 01-EI-0046

Active Accrual, Protocols Recruiting New Patients

Title:
Evaluation and Treatment of Corneal and External Diseases and Anterior Segment Disorders
Number:
01-EI-0046
Summary:
This study offers evaluation and treatment for patients with certain corneal and external diseases of the eye (diseases of the surface of the eye and its surrounding structures). The protocol is not designed to test new treatments; rather, patients will receive current standard of care treatments. The purpose of the study is twofold: 1) to allow National Eye Institute physicians to increase their knowledge of various corneal and external conditions and identify possible new avenues of research in this area; and 2) to establish a pool of patients who may be eligible for new studies as they are developed. (Participants in this protocol will not be required to join a new study; the decision will be voluntary.)

Children and adults with corneal or external eye diseases may be eligible for this study. Candidates will be screened with a medical history, brief physical examination, thorough eye examination and blood test. The eye examination includes measurements of eye pressure and visual acuity (ability to see the vision chart) and dilation of the pupils to examine the lens and retina (back part of the eye). Patients will also undergo the following procedures:

1. Eye photography - Special photographs of the inside of the eye to help evaluate the status of the cornea and conjunctiva (the most superficial layer of the eye) evaluate changes that may occur in the future. From two to 20 pictures may be taken, depending on the eye condition. The camera flashes a bright light into the eye for each picture.

2. Conjunctival or lacrimal gland biopsy - A small piece of the conjunctiva or the lacrimal (tear) gland, is removed for examination under the microscope. Anesthetic drops and possibly an injection of anesthetic are given to numb the eye. An antibiotic ointment and patch may be placed over the eye for several hours after the procedure.

Participants will be followed at least 3 years. Follow-up visits are scheduled according to the standard of care for the individual patient's eye problem. Vision will be checked at each visit, and some of the tests described above may be repeated to follow the progress of disease and evaluate the response to any treatment that is given.

Sponsoring Institute:
National Eye Institute (NEI)
Recruitment Detail
Type: Participants currently recruited/enrolled
Gender: Male & Female
Referral Letter Required: No
Population Exclusion(s): None

Eligibility Criteria:
INCLUSION CRITERIA:

1. Corneal and external diseases or anterior segment disorders.

2. If adult, ability to provide informed consent. Cognitively impaired adults will not be enrolled.

3. Infants under the age of 2 years are excluded. Children greater than or equal to age of 2 years willing to provide assent who meet other study requirements are eligible to participate.

EXCLUSION CRITERIA:

Subjects may be excluded if they

1. Are unwilling or unable to cooperate with study procedures.

2. Have any disease or condition with less than 3 year expected survival.

3. There are no medical exclusions.

Special Instructions:
Currently Not Provided
Keywords:
Keratitis
Conjunctivitis
Meibomitis
Corneal Infiltrates
Dacryocystitis
Blepharitis
Dacryoadenitis
Recruitment Keyword(s):
Corneal Eye Disease
Keratitis
Blepharitis
Condition(s):
Blepharitis
Conjunctivitis
Corneal Disease
Dacryoadenitis
Dacryocystitis
Keratitis
Investigational Drug(s):
None
Investigational Device(s):
None
Intervention(s):
None
Supporting Site:
National Eye Institute

Contact(s):
Patient Recruitment and Public Liaison Office
Building 61
10 Cloister Court
Bethesda, Maryland 20892-4754
Toll Free: 1-800-411-1222
TTY: 301-594-9774 (local),1-866-411-1010 (toll free)
Fax: 301-480-9793

Electronic Mail:prpl@mail.cc.nih.gov

Citation(s): Not Provided

Active Accrual, Protocols Recruiting New Patients

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