retinitis
retinitis
Explore linked clinical trials. Standard reference: MONDO:00027087 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Evaluation of Safety and Efficacy of Autologous LB-DTK-CMV in Patients With Antiviral-Resistant and Refractory Cytomegalovirus Retinitis. | DNA Virus Infections, Hemic and Lymphatic Diseases, Herpesviridae infectious disease, Infections, Neoplasms by Site, autoimmune disease, cytomegalovirus infection, cytomegalovirus retinitis, eye disorder, eye infectious disorder, hematologic disorder, hematopoietic and lymphoid system neoplasm, immune system disorder, neoplasm, retinal disorder, retinitis, viral eye infection, viral infectious disease | Recruiting | Not applicable | 2026-07-01 | NCT07679412 | |
| Birdshot Chorioretinopathy : Prospective Follow-up and Immunogenetic Studies(CO-BIRD) | White Dot Syndromes, autoimmune disease, birdshot chorioretinopathy, chorioretinitis, choroiditis, eye disorder, immune system disorder, optic choroid disorder, panuveitis, posterior uveitis, retinal disorder, retinitis, uveal disorder, uveitis | Recruiting | Not stated | 2026-03-04 | NCT05153057 | |
| Quantification & Classification of Inflammatory Cells in Uveitis Using OCT | Behcet disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA Virus Infections, Hemic and Lymphatic Diseases, Herpesviridae infectious disease, Hypersensitivity, Delayed, Infections, Posterior Vitreous Detachment, Skin Diseases, Viral, Skin and Connective Tissue Diseases, Spondylarthritis, Stomatognathic Diseases, White Dot Syndromes, anterior uveitis, arthritic joint disease, arthropathy, autoimmune disease, birdshot chorioretinopathy, bone disorder, cardiovascular disorder, chorioretinitis, choroiditis, connective tissue disorder, eye disorder, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, herpes simplex infectious disease, immune system disorder, juvenile idiopathic arthritis, lymphatic system disorder, lymphoproliferative syndrome, mouth disorder, musculoskeletal system disorder, optic choroid disorder, panuveitis, posterior uveitis, retinal disorder, retinitis, rheumatic disorder, sarcoidosis, skin disorder, skin disorder caused by infection, skin vascular disease, spondylitis, uveal disorder, uveitis, vascular disorder, vasculitis, vertebral column disorder, viral infectious disease, vitreous detachment | Recruiting | Not stated | 2025-07-17 | NCT07065747 | |
| Non-Interventional Long Term Follow-up Study of Participants Previously Enrolled in the RESTORE Study | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Vision, Low, eye disorder, hereditary disease, inherited retinal dystrophy, nervous system disorder, retinal degeneration, retinal disorder, retinitis, retinitis pigmentosa, vision disorder | Active, not recruiting | Not stated | 2025-03-24 | NCT06162585 | |
| Natural History Study of Retinitis Pigmentosa Type 11 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis, retinitis pigmentosa, retinitis pigmentosa 11 | Active, not recruiting | Not stated | 2025-03-21 | NCT04805658 | |
| Clinical Study of High Concentration Ganciclovir Eye Drops in the Treatment of Cytomegalovirus Retinitis | DNA Virus Infections, Herpesviridae infectious disease, Infections, cytomegalovirus infection, cytomegalovirus retinitis, eye disorder, eye infectious disorder, retinal disorder, retinitis, viral eye infection, viral infectious disease | Recruiting | Early phase 1 | 2023-06-23 | NCT05911503 | |
| A Study to Evaluate the Safety and Tolerability of QR-1123 in Subjects With Autosomal Dominant Retinitis Pigmentosa Due to the P23H Mutation in the RHO Gene | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, congenital stationary night blindness autosomal dominant 1, contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A, eye disorder, hereditary disease, inherited retinal dystrophy, nervous system disorder, retinal degeneration, retinal disorder, retinitis, retinitis pigmentosa, vision disorder | Active, not recruiting | Phase 1 / Phase 2 | 2022-05-06 | NCT04123626 |