corneal dystrophy

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Information
Disease name
corneal dystrophy
Disease ID
DOID:2566
Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT04424550 Completed Comparative Results After DSAEK, UT-DSAEK and DMEK for Fuchs Endothelial Corneal Dystophy August 1, 2017 August 1, 2019
NCT04484402 Completed Phase 1/Phase 2 Treatment of Patients With Inflammatory-dystrophic Diseases of the Cornea Using Autologous Stem Cells October 3, 2016 December 30, 2019
NCT05279157 Completed Phase 2 Autologous Adipose-Derived Adult Stem Cell Implantation for Corneal Diseases (ADASCs-CT-CD) April 19, 2022 February 5, 2023
NCT05891106 Completed AONDA Therapeutic Indication Study I June 28, 2023 July 10, 2023
NCT05927740 Completed N/A The Efficacy of Hyperemesis Gravidarum on Macular Thickness, Corneal Thickness and Intraocular Pressure in Pregnancy March 10, 2020 May 11, 2023
NCT05956535 Enrolling by invitation Air Optix® Night and Day® Aqua Therapeutic Wear September 26, 2023 July 2024
NCT03504800 Recruiting OCT in Diagnosis of Irregular Corneas May 1, 2018 April 2026
NCT04384094 Unknown status Defining the Operating Parameters for a Rebound-esthesiometer August 2020 December 2020
NCT02736877 Unknown status N/A Corneal Transplantation Guided by OCT RESCAN April 2016 March 2017
NCT02746055 Unknown status Study of the Prevalence of TGFBI Corneal Dystrophies April 2016 April 2017
NCT03461991 Unknown status N/A Correlation Between In-vivo Anatomy of Corneal Dystrophies as Assessed by High- Resolution Optical Coherence Tomography (OCT) Measurement and Histological Examination August 21, 2018 September 2, 2023
NCT04129021 Unknown status N/A Multimodal Ophthalmic Imaging July 15, 2019 June 30, 2023
NCT01084850 Unknown status Corneal Endothelium Morphology and Central Thickness in Type II Diabetes Mellitus and Normal Subjects June 2009 September 2010
Disase is a (Disease Ontology)
DOID:10124
Cross Reference ID (Disease Ontology)
ICD10CM:H18.5
Cross Reference ID (Disease Ontology)
ICD9CM:371.5
Cross Reference ID (Disease Ontology)
MESH:D003317
Cross Reference ID (Disease Ontology)
NCI:C34512
Cross Reference ID (Disease Ontology)
NCI:C34513
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:5587004
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:77797009
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0010035
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0010036
HPO alt_id (Human Phenotype Ontology)
HP:0007775
HPO Human Phenotype ID (Human Phenotype Ontology)
HP:0001131
OrphaNumber from OrphaNet (Orphanet)
34533