Page 1 of Clinical Trials for "Eye Diseases, Hereditary", 151 Total Matches
- 1CompletedLast Updated: December 18, 2008Condition(s): Eye Diseases, Hereditary
- 2Enrolling by invitationLast Updated: December 28, 2011Condition(s): Retinitis Pigmentosa; Retinal Diseases; Eye Diseases; Eye Disease, Hereditary; Retinal Degeneration
- 3CompletedLast Updated: March 5, 2008Condition(s): Hereditary Eye Disease
- 4CompletedLast Updated: May 21, 2008Condition(s): Hereditary Eye Disease
- 5RecruitingLast Updated: April 19, 2012Condition(s): Choroidal Neovascularization; Myopia; Punctate Inner Choroidopathy (PIC); Multifocal Choroiditis; Ocular Histoplasmosis Syndrome; Central Serous Chorioretinopathy (CSC); Angioid Streaks; Trauma, or Hereditary Eye Diseases
- 6RecruitingLast Updated: July 28, 2011Condition(s): Muscular Dystrophy; Congenital Muscular Dystrophy; Fukutin-related Protein Gene; Limb Girdle; FKRP Gene; Childhood Onset LGMD; Adult Onset LGMD; POMT1; POMT2; POMGnT1; LARGE; Alpha Dystroglycan; Dystroglycanopathy; Centronuclear; Multiminicore; Multicore; Minicore; Congenital Fiber Type Disproportion; Myotubular; Nemaline; Congenital Myopathy; Neuromuscular; Rigid Spine; Phenotype-Genotype Correlation; Cough Assisted Device; Neuromuscular Disease; Respiratory Exacerbation; Invasive Ventilation; Chest Physiotherapy; Congenital Myopathies; Genetic Mutations; Hypertrophic Cardiomyopathy; Wheelchair Use; Cataract; Opthalmoplegia; Ullrich Congenital Muscular Dystrophy; Intermediate Collagen VI Myopathy; Laminin Alpha 2 Related Congenital Muscular Dystrophy; MDC1A; Merosin Deficient Congenital Muscular Dystrophy; Congenital Muscular Dystrophy Undiagnosed; Congenital Muscular Dystrophy Merosin Positive; Walker Warburg Syndrome; Muscle Eye Brain Disease; Fukuyama; Integrin Alpha 7 Deficiency; Integrin Alpha 9 Deficiency; Laminopathy; Lamin AC; SEPN 1 Related Myopathies; Bethlem Myopathy; Dystroglycanopathies; LGMD2K; LGMD2I; LGMD2L; LGMD2N; Actin Aggregation Myopathy; Cap Disease; Central Core Disease; Centronuclear Myopathy; Core Rod Myopathy; Hyaline Body Myopathy; Multiminicore Myopathy; Myotubular Myopathy; Nemaline Myopathy; Tubular Aggregate Myopathy; Zebra Body Disease Myopathy; Congenital Myopathy Other; Reducing Body Myopathy; Sarcotubular Myopathy; Spheroid Body Myopathy
- 7RecruitingLast Updated: December 19, 2011Condition(s): Retinitis Pigmentosa; Retinal Degeneration
- 8Active, not recruitingLast Updated: June 6, 2011Condition(s): Retinitis Pigmentosa
- 9RecruitingLast Updated: October 21, 2011Condition(s): Graves´ Disease
- 10CompletedLast Updated: November 10, 2008Condition(s): Retinitis Pigmentosa
- 11Active, not recruitingLast Updated: April 5, 2012Condition(s): Retinitis Pigmentosa
- 12CompletedLast Updated: May 3, 2012Condition(s): Retinitis Pigmentosa; Macula Off; Primary Open Angle Glaucoma; Hereditary Macular Degeneration; Treated Retina Detachment; Retinal Artery Occlusion; Retinal Vein Occlusion; Non-Arthritic-Anterior-Ischemic Optic-Neuropathy; Hereditary Autosomal Dominant Optic Atrophy; Dry Age Related Macular Degeneration; Ischemic Macula Edema
- 13Active, not recruitingLast Updated: February 9, 2012Condition(s): Graves Ophthalmopathy
- 14RecruitingLast Updated: November 30, 2011Condition(s): Retinitis Pigmentosa; Cone-rod Dystrophy; Macular Degeneration
- 15RecruitingLast Updated: December 9, 2010Condition(s): Brain Disorders; Aicardi Syndrome
- 16Enrolling by invitationLast Updated: October 19, 2011Condition(s): Spinal Cord Injury; Cervical Spondylosis With Myelopathy; Degenerative Disorder
- 17RecruitingLast Updated: May 16, 2012Condition(s): Albinism; Oculocutaneous Albinism; Foveal Hypoplasia; Hypopigmentation; Nystagmus
- 18RecruitingLast Updated: March 1, 2012Condition(s): RP (Retinitis Pigmentosa)
- 19RecruitingLast Updated: March 20, 2012Condition(s): WAGR Syndrome; Wilm's Tumor; Aniridia; Urogenital Abnormalities; Mental Retardation
- 20RecruitingLast Updated: August 18, 2011Condition(s): Aniridia
Clinical Trials content is provided directly by the U.S. National Institutes of Health via ClinicalTrials.gov and is not reviewed separately by ClinicalTrialsFeeds.org. Every page of specific clinical trials information contains a unique identifier which can be used to find further details directly from the National Institutes of Health.
The URL of this page is: http://clinicaltrialsfeeds.org/clinical-trials/results/?cond=%22Eye+Diseases%2C+Hereditary%22
