Genetic Analysis of Chronic Central Serous Chorioretinopathy Masquerading as Neovascular AMD
NCT01880788 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 152
Last updated 2015-09-18
Summary
The study will be designed as a case control evaluation to compare the genetic profiles of three groups of patients categorized according to diagnosis.
Group 1 - CNV secondary to CSC Group 2 - CSC without CNV Group 3 - CNV secondary to advanced AMD.
Conditions
- Age Related Macular Degeneration
- Choroidal Neovascularization
- Central Serous Chorioretinopathy
Sponsors & Collaborators
-
Vitreous -Retina- Macula Consultants of New York
collaborator OTHER -
Sequenom, Inc.
lead INDUSTRY
Eligibility
- Min Age
- 30 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-11-30
- Primary Completion
- 2015-03-31
- Completion
- 2015-08-31
Countries
- United States
Study Locations
More Related Trials
-
Molecular Analysis of Microphthalmia/Anophthalmia
NCT00011843 ·Status: COMPLETED
-
Genetic Analysis of Uncommon Disease Presentations in Non-US Populations
NCT06595940 ·Status: RECRUITING
-
Identification of Genomic Loci Determining Susceptibility to the Development of High Myopia
NCT02583620 ·Status: COMPLETED ·Phase: NA
-
Diagnostic and Screening Study of Genetic Disorders
NCT00006057 ·Status: COMPLETED
-
Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype Correlation
NCT02886611 ·Status: RECRUITING
-
Genetic Identification of Monogenic Disorders in Early-onset Stroke Using Targeted Next Generation Sequencing Panel
NCT04485598 ·Status: COMPLETED
-
Genetics of Inherited Eye Disease
NCT02471287 ·Status: RECRUITING
-
Study of New Mutations in Cone Disorders
NCT04658251 ·Status: TERMINATED
-
Primary Hyperoxaluria Mutation Genotyping
NCT00589225 ·Status: COMPLETED
-
Genetic Diagnosis in Congenital Cataracts
NCT05782452 ·Status: COMPLETED
-
Genome-wide Analysis of Single Nucleotide Polymorphisms of Brain Arteriovenous Malformations and Cerebral Aneurysm
NCT01801488 ·Status: TERMINATED
-
Genetic, Metabolic, and Growth Factor Repository for Cerebrovascular Disorders
NCT02910180 ·Status: RECRUITING
-
The Genetic Characterization of Dementia
NCT01867359 ·Status: COMPLETED
-
Genetic Studies of Early-onset Dementia
NCT04906863 ·Status: RECRUITING
-
Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing
NCT02558478 ·Status: UNKNOWN
-
Adult Patients With Undiagnosed Conditions and Their Responses to Clinically Uncertain Results From Exome Sequencing
NCT03605004 ·Status: COMPLETED
-
Mechanisms of Inherited Retinal Dystrophies Using Whole Genome Sequencing and in Vitro and in Vivo Models
NCT05793515 ·Status: COMPLETED
-
Rare and Undiagnosed Disease Research Biorepository
NCT04703179 ·Status: ENROLLING_BY_INVITATION
-
Clinical and Molecular Studies in Families With Inherited Eye Disease
NCT02771236 ·Status: RECRUITING
-
Identification and Characterization of Novel Non-Coding Variants That Contribute to Genetic Disorders
NCT04399694 ·Status: COMPLETED
-
Genetic Variants in Nicotinamide Adenine Dinucleotide (NAD) Synthesis Pathway
NCT03799705 ·Status: COMPLETED
-
Structural Chromosome Rearrangements and Brain Disorders
NCT06072079 ·Status: ENROLLING_BY_INVITATION
-
The Clinical Study of Sex Chromosome Variants
NCT01661010 ·Status: COMPLETED
-
MIRAGE: Multi-Institutional Research in Alzheimer's Genetic Epidemiology
NCT00239759 ·Status: COMPLETED
-
Psychiatric Genotype/Phenotype Project Repository
NCT00762866 ·Status: ENROLLING_BY_INVITATION