Subfoveal Choroidal Neovascularization Clinical Trial
Official title:
Randomized, Double Blind, Controlled Study With Verteporfin Photodynamic Therapy And Intravitreal Triamcinolone(IVTA) Vs Triple Therapy With Verteporfin Photodynamic Therapy, Intravitreal Triamcinolone And Intravitreal Ranibizumab In Patients With Subfoveal Choroidal Neovascularization(CNV) Secondary To Age-related Macular Degeneration(AMD)
Verified date | May 2024 |
Source | Asociación para Evitar la Ceguera en México |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to compare the efficacy of photodynamic therapy with verteporfin (PDT) and IVTA vs triple therapy (TT) in patients with subfoveal choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD). The investigators designed a prospective, comparative, randomized, double blind, controlled study. 15 patients with classic subfoveal choroidal neovascularization secondary to age-related macular degeneration were randomized. Triple therapy can potentially offer a new treatment modality for choroidal neovascularization in patients with macular degeneration and other diseases.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | September 2006 |
Est. primary completion date | April 2006 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years to 90 Years |
Eligibility | Inclusion Criteria: - Subfoveal choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD) - Any visual acuity Exclusion Criteria: - Previous treatment - Glaucoma |
Country | Name | City | State |
---|---|---|---|
Mexico | Centro Medico Isemmym | Metepec | Estado-de-Mexico |
Lead Sponsor | Collaborator |
---|---|
Asociación para Evitar la Ceguera en México | Centro Medico Issemym |
Mexico,
Arias L, Garcia-Arumi J, Ramon JM, Badia M, Rubio M, Pujol O. Photodynamic therapy with intravitreal triamcinolone in predominantly classic choroidal neovascularization: one-year results of a randomized study. Ophthalmology. 2006 Dec;113(12):2243-50. doi: 10.1016/j.ophtha.2006.04.039. Epub 2006 Sep 25. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The main outcome measures were visual acuity (VA) | |||
Primary | mean change in lesion size | |||
Primary | mean change in foveal thickness | |||
Secondary | retreatment rate | |||
Secondary | the incidence and severity of adverse events |
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT02599064 -
Evaluating RXI-109 to Reduce the Progression of Subretinal Fibrosis in Subjects With NVAMD
|
Phase 1/Phase 2 | |
Terminated |
NCT01122511 -
Safety and Efficacy of Dexamethasone as Adjunctive Therapy to Ranibizumab in Subjects With Choroidal Neovascularization and Age-Related Macular Degeneration
|
Phase 2 |