Family Studies of Uveal Coloboma
NCT00368004 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 100
Last updated 2019-12-17
Summary
This study will identify the genes responsible for uveal coloboma, an abnormal development of the eye caused by incomplete closure of a normally-occurring gap in the eye (the optic fissure) after the fifth week of life in a human embryo. There have been studies of families in which more than one person has been affected by this disorder. Coloboma occurs in about 1 of 10,000 live births and may cause significant vision loss. Researchers seek a better understanding of the genes responsible for this disorder.
Adults and children who have more than one member of the family with uveal coloboma may be eligible for this study. Patients will undergo a detailed medical history and eye examination appropriate for their age. The pupils will be dilated, through the use of eye drops. Dilation will continue for 4 to 6 hours, and wearing of sunglasses can reduce temporary glare that many patients may experience in brightly lit areas. In addition, pictures will be taken of the front or back of the eye, a procedure that also involves dilation of the pupils. Patients who have coloboma will undergo a complete physical examination. Blood samples will be collected, with a total of about 2 tablespoons from patients ages 10 and older and about 1 teaspoon for each 5 pounds of body weight for younger patients. Also, patients with coloboma may be asked to undergo X-rays , ultrasound, or other tests that are medically indicated.
To have enough DNA to study, the researchers may create a cell line to grow more DNA. Laboratory samples will be coded so that there is no identifying information about participants in this study. No other testing or research will be done on blood samples collected unless patients give permission. The researchers will not provide information about patients' health to other people without your express permission.
Conditions
- Coloboma
Sponsors & Collaborators
-
National Eye Institute (NEI)
lead NIH
Principal Investigators
-
Brian P Brooks, M.D. · National Eye Institute (NEI)
Eligibility
- Max Age
- 100 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2006-07-28
- Completion
- 2013-04-15
Countries
- United States
Study Locations
More Related Trials
-
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies
NCT03059420 ·Status: RECRUITING
-
Screening for Studies on Inherited Eye Diseases
NCT00001732 ·Status: COMPLETED
-
Potential Research Participants for Future Studies of Inherited Eye Diseases
NCT00559234 ·Status: COMPLETED
-
Early Visual Functions in Patients at Risk of Developing Cerebral Visual Impairment. A Pilot Study
NCT05865093 ·Status: RECRUITING
-
Validation of a Parental Questionnaire for Screening Children for Neurovisual Disorders
NCT06997354 ·Status: RECRUITING
-
Validation of the GoCheck Kids® Eye Screeningtest in Infants in Flanders
NCT05484453 ·Status: ACTIVE_NOT_RECRUITING
-
Early Detection and Prevention of Amblyopia and Visual Impairment Through Systematic Pediatric Vision Screening
NCT07112560 ·Status: NOT_YET_RECRUITING
-
Cerebral/ Cortical Visual Impairment: Screening, Identification and Outcome Prediction in Neonates
NCT07275021 ·Status: RECRUITING
-
Early Versus Delayed Surgery for Infantile Esotropia
NCT01166503 ·Status: COMPLETED
-
Determining Whether Multiple Anesthesia Exposures Affect Cognitive Function for Retinoblastoma Patients
NCT03546387 ·Status: RECRUITING
-
Photic Blink Reflex in People With Blepharospasm and Increased Blinking
NCT03263000 ·Status: TERMINATED
-
Neurovascular Coupling in Subjects With Amblyopia
NCT01746693 ·Status: UNKNOWN ·Phase: NA
-
Brain Changes in Blepharospasm
NCT00500799 ·Status: COMPLETED
-
Evaluation and Treatment of Pediatric Eye Diseases
NCT00006422 ·Status: COMPLETED ·Phase: NA
-
Eye-Hand Coordination in Children With Spastic Diplegia
NCT00024791 ·Status: COMPLETED
-
Biological Clock Dysfunction in Optic Nerve Hypoplasia
NCT00825591 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
Human Samples and Data Repository
NCT00539370 ·Status: TERMINATED
-
Pupillometry for the Prediction of Neurologic Outcomes in Severe Traumatic Brain Injury
NCT02465242 ·Status: UNKNOWN
-
Evaluation of the Diagnostic Value of Video-oculography in CANVAS Neuronopathies
NCT05278091 ·Status: COMPLETED
-
MRI Screening for Auditory Pathway Malformations in Visually Impaired Children
NCT02896738 ·Status: COMPLETED
-
People s Expectations When Enrolling in a Phase I/II RS1 Ocular Gene Transfer Clinical Trial
NCT02317354 ·Status: COMPLETED
-
Gocheck Kids vs. Welch Allyn Spot Vision Screener
NCT04321538 ·Status: COMPLETED
-
Screening for Research Participants
NCT00655096 ·Status: RECRUITING
-
Vision In Preschoolers Study (VIP Study)
NCT00038753 ·Status: UNKNOWN ·Phase: PHASE3
-
Outcome pRognostication of Acute Brain Injury With the NeuroloGical Pupil indEx
NCT04490005 ·Status: COMPLETED