retinoschisis
Information
- Disease name
- retinoschisis
- Disease ID
- DOID:8465
- 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 |
|---|---|---|---|---|---|
| NCT02317887 | Active, not recruiting | Phase 1/Phase 2 | Study of RS1 Ocular Gene Transfer for X-linked Retinoschisis | February 11, 2015 | July 31, 2025 |
| NCT00055029 | Active, not recruiting | Clinical and Genetic Studies of X-Linked Juvenile Retinoschisis | May 19, 2003 | ||
| NCT02317354 | Completed | People s Expectations When Enrolling in a Phase I/II RS1 Ocular Gene Transfer Clinical Trial | December 13, 2014 | November 20, 2017 | |
| NCT02682797 | Completed | Optical Coherence Tomography Evaluation of Retinoschisis and Retinal Detachment | September 2013 | July 2016 | |
| NCT01995045 | Completed | Phase 4 | Postoperative Pain Control Following Vitreoretinal Surgery | July 2012 | December 2015 |
| NCT03023800 | Completed | N/A | Effects of Macular Buckle Versus Vitrectomy on Macular Schisis and Macular Detachment in Highly Myopic Eyes | April 2015 | October 12, 2017 |
| NCT03354403 | Completed | Mothers Experiences With X-linked Retinoschisis Compared to Fathers Experiences | December 1, 2017 | October 30, 2019 | |
| NCT06289452 | Recruiting | Early Phase 1 | Safety and Efficacy Study of IVB102 Injection in Subjects With X-linked Retinoschisis | March 8, 2024 | December 31, 2029 |
| NCT02435940 | Recruiting | Inherited Retinal Degenerative Disease Registry | June 2014 | June 2037 | |
| NCT06114537 | Recruiting | Phase 2 | The AXIS Study: the Efficacy of Acetazolamide for the Treatment of Cystoid Fluid Collections in Retinoschisis | January 20, 2023 | March 20, 2025 |
- Disase is a (Disease Ontology)
- DOID:8466
- Cross Reference ID (Disease Ontology)
- ICD10CM:H33.10
- Cross Reference ID (Disease Ontology)
- ICD9CM:361.10
- Cross Reference ID (Disease Ontology)
- MESH:D041441
- Cross Reference ID (Disease Ontology)
- NCI:C85046
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:389992006
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0152439
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0030502
- MedGen concept unique identifier (MedGen Concept name)
- C0152439
- MedGen unique identifier (MedGen Concept name)
- 56292
- MeSH unique ID (MeSH (Medical Subject Headings))
- D041441