Sildenafil for Treatment of Choroidal Ischemia
Primary Purpose
Choroidal Ischemia, Vitelliform Macular Dystrophy, Age-related Macular Degeneration
Status
Active
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Sildenafil
Standard of Care Sildenafil
Ocular Coherence Tomography-Angiography (OCT-A)
Visual Acuity (VA)
Sponsored by
About this trial
This is an interventional treatment trial for Choroidal Ischemia focused on measuring Sildenafil, Viagra, Revatio
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of retinal and choroidal degenerations (reticular or vitelliform AMD or vitelliform-type subretinal drusen) or hereditary or acquired retinal dystrophies (retinitis pigmentosa or central serous retinopathy)
Exclusion Criteria:
- Diagnosis of heart disease requiring use of nitrates
- Inability to be examined monthly or bi-monthly
Sites / Locations
- Columbia University Medical Center, Edward Harkness Eye Institute
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Standard of Care Sildenafil
Sildenafil
Arm Description
Medical record review for participants that are prescribed Sildenafil off-label as part of standard of care treatment for disease.
Participants are prescribed sildenafil 40-80 mg daily.
Outcomes
Primary Outcome Measures
Change in Choroidal Perfusion
Patients are evaluated for progression of disease/dystrophy via visual acuity (improved/stable/worsened) and appearance of fluid layer and drusen on OCT testing.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04356716
Brief Title
Sildenafil for Treatment of Choroidal Ischemia
Official Title
Sildenafil for Treatment of Choroidal Ischemia
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 11, 2014 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Columbia University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The hypothesis of this study is to determine if there is a benefit afforded by the use of systemic Sildenafil to patients with choroidal and retinal degenerations and dystrophies, such as vitelliform degeneration, dry and reticular age-related macular degeneration (AMD) as well as patients with hereditary and acquired retinal dystrophies such as retinitis pigmentosa and central serous retinopathy.
Detailed Description
Age-Related Macular Degeneration (AMD) is a sight-threatening visual disturbance that affects the macula in older ages. It is irreversible if the pigment epithelium is lost (dry AMD), but wet AMD can be arrested or delayed with the use of intraocular injections of one of 3 different compounds. All three drugs are injected into the eye in minute doses of usually 0.1 ml. These are usually injected at 4 to 6 week intervals and treatment may be extended for several years. Different patterns of injection times are followed but usually are monthly for 12 or more months, or monthly for 3 months and then extended observation at one to two month intervals unless vision (visual acuity) declines or Optical Coherence Tomography-angiography (OCT-A) shows recurrence of fluid or increase in size or amount of drusen (deposits of lipofuscin) in the retina. Vitelliform macular degeneration is a disorder that causes visual loss due to drusen in the macula, which have been shown to be identical to the deposits seen in macular degeneration. The goal of therapy in this proposal is to use sildenafil to increase choroidal blood flow to treat dry AMD and slow the progression of visual loss in vitelliform and age-related dry AMD as well as other macular, retinal and choroidal degenerations and dystrophies, as well as reduce or eliminate the number of injections required by slowing down transformation of dry AMD to wet AMD in treated patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Choroidal Ischemia, Vitelliform Macular Dystrophy, Age-related Macular Degeneration, Central Serous Retinopathy, Retinitis Pigmentosa
Keywords
Sildenafil, Viagra, Revatio
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Participants are assigned to the investigational sildenafil arm with a dose of 40-80mg daily, or the records review arm when taking sildenafil off-label.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
25 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Standard of Care Sildenafil
Arm Type
Active Comparator
Arm Description
Medical record review for participants that are prescribed Sildenafil off-label as part of standard of care treatment for disease.
Arm Title
Sildenafil
Arm Type
Active Comparator
Arm Description
Participants are prescribed sildenafil 40-80 mg daily.
Intervention Type
Drug
Intervention Name(s)
Sildenafil
Other Intervention Name(s)
Viagra, Revatio
Intervention Description
Initial Sildenafil dosage will be weight dependent. Participants will start at 40 mg daily (20mg in the morning, 20 mg in the evening) or 60 mg daily (40mg in the morning and 20 mg in the evening). Sildenafil dosage may be increased to up to 80mg daily (20-40mg in the morning and 20-40mg in the evening) based on the response to lower doses. If the participant has not had improvement after initial treatment, the dose may be increased, at the discretion of the study physician.
Intervention Type
Other
Intervention Name(s)
Standard of Care Sildenafil
Other Intervention Name(s)
Viagra, Revatio
Intervention Description
Medical record review of participants that receive Sildenafil as part of standard of care.
Intervention Type
Diagnostic Test
Intervention Name(s)
Ocular Coherence Tomography-Angiography (OCT-A)
Intervention Description
Retinal photographs will be taken at each study visit.
Intervention Type
Other
Intervention Name(s)
Visual Acuity (VA)
Intervention Description
Visual acuity will be measured with Snellen Eye Chart at each study visit.
Primary Outcome Measure Information:
Title
Change in Choroidal Perfusion
Description
Patients are evaluated for progression of disease/dystrophy via visual acuity (improved/stable/worsened) and appearance of fluid layer and drusen on OCT testing.
Time Frame
Up to 5 Years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of retinal and choroidal degenerations (reticular or vitelliform AMD or vitelliform-type subretinal drusen) or hereditary or acquired retinal dystrophies (retinitis pigmentosa or central serous retinopathy)
Exclusion Criteria:
Diagnosis of heart disease requiring use of nitrates
Inability to be examined monthly or bi-monthly
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Donald Jackson Coleman, MD
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Columbia University Medical Center, Edward Harkness Eye Institute
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
23740965
Citation
Coleman DJ, Silverman RH, Rondeau MJ, Lloyd HO, Khanifar AA, Chan RV. Age-related macular degeneration: choroidal ischaemia? Br J Ophthalmol. 2013 Aug;97(8):1020-3. doi: 10.1136/bjophthalmol-2013-303143. Epub 2013 Jun 5.
Results Reference
background
PubMed Identifier
29694963
Citation
Coleman DJ, Lee W, Chang S, Silverman RH, Lloyd HO, Daly S, Tsang SH. Treatment of Macular Degeneration with Sildenafil: Results of a Two-Year Trial. Ophthalmologica. 2018;240(1):45-54. doi: 10.1159/000486105. Epub 2018 Apr 25.
Results Reference
background
Learn more about this trial
Sildenafil for Treatment of Choroidal Ischemia
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