Familial Exudative Vitreoretinopathies
Familial Exudative Vitreoretinopathies
Explore linked clinical trials. Standard reference: MESH:M0006471121 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Safety and Efficacy of 18 mm Short Vitrectomy Probe for Pediatric Vitreoretinal Surgeries | Coats disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Abnormalities, Eye Diseases, Hereditary, Familial Exudative Vitreoretinopathies, cardiovascular disorder, eye disorder, hereditary disease, persistent hyperplastic primary vitreous, retinal disorder, retinal vascular disorder, telangiectasis, vascular disorder, vitreous disorder | Recruiting | Phase 4 | 2024-07-25 | NCT06520410 |