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Optical Coherence Tomography Angiography (OCTA) - Directed PDT Triple Therapy

Megadott ok: IRB stopped study due to safety concerns before any participants were enrolled.

Key facts

Where
Winston-Salem, Egyesült ÁllamokSee the site
Phase
4. fázis

Where in Egyesült Államok

  • Wake Forest Health SciencesWinston-Salem, Egyesült ÁllamokNo longer taking part

Trial details

Who runs it
Wake Forest University Health Sciences
Trial code
NCT04075136
Record updated
2024. március 22.
Original description
Optical Coherent Tomography Angiography (OCTA)-Directed PDT Triple Therapy for Treatment-Naïve Patients with Exudative Age-related Macular Degeneration (ARMD) versus Standard of Care Anti-VEGF MonotherapyRead full original descriptionShow less

OCTA-Directed PDT Triple Therapy for Treatment-Naïve Patients With Exudative Age-Related Macular Degeneration Versus Standard of Care Anti-VEGF(Anti-vascular Endothelial Growth Factor) Monotherapy

Optical Coherent Tomography Angiography (OCTA)-Directed PDT Triple Therapy for Treatment-Naïve Patients with Exudative Age-related Macular Degeneration (ARMD) versus Standard of Care Anti-VEGF Monotherapy

Inclusion: Willing to give written informed consent; Willing and able to comply with all study procedures for the duration of the study; Presence of Exudative ARMD with evidence of choroidal neovascularization: type 1, 2, and/or 3 on spectral domain OCT, fluorescein angiography, indocyanine green angiogram and optical coherent tomography angiography; Visual Acuity of 20/25 to 20/400 at screening and baseline visits using an autorefractor or Early Treatment Diabetic Retinopathy Study; Intraocular pressure less than or equal to 25mmHG; Females of childbearing potential that are willing to use medically acceptable methods of birth control.

Exclusion: Previous treatment with macular photocoagulation, anti-VEGF medication or PDT with Visudyne; Previous vitrectomy; Have received previous treatment for ARMD; Myocardial infarction or cerebrovascular accident within the last 6 weeks; Allergies to fluorescein and indocyanine, dilating agents or anti-VEGF medications; Any uncontrolled condition or illness that in the opinion of the investigator makes the subject unsuitable for the study; Exudation maculopathies without drusen; Optic neuropathy; Diabetic retinopathy; Traction maculopathies.

ClinicalTrials.gov NCT04075136