GUARDIAN: A Single-Center Trial of High Frequency Pegaptanib for Rapid Restoration of VEGF Levels in Diabetic Retinal Edema
Study Details
Study Description
Brief Summary
Establish the efficacy of initial high frequency loading of intravitreal pegaptanib bi-weekly during the initial treatment period when the VEGF levels are the greatest and then gradually extending the administration frequency to monthly as homeostasis ensues for the treatment of DME, as measured by best-corrected visual acuity.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
Determine if high frequency loading intravitreal pegaptanib will reduce the area and/or volume of DME, as assessed by Spectral Domain optical coherence tomography (SD-OCT) and to determine if this loading with gradual taper schedule of intravitreal pegaptanib will reduce the need for macular laser treatment.
Study Design
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Inclusion Criteria:
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Type I or Type II diabetics, with an age of 18 years of older
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Vision of 20/40-20/400 in the Study Eye
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Diabetic Macular Edema as documented by SD-OCT and Fluorescein Angiogram.
Exclusion Criteria:
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Cannot attened all trail required visits
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Eyes in which retinal surgery is needed now are is likely to be needed within 6 months, which the surgeon believes will not respond to non-surgical intervention.
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Presence of any abnormality that is likely to confound assessment of visual acuity improvement in eyes in which macular edema resolves, or improves, such as non-perfusion greater than 1 disc area involving the foveal avascular zone, epiretinal membrane associated with signs of contraction and/or significant opacification, or presence of chorioretinal atrophy involving the center of the macula.
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Vitreomacular traction determined clinically and/or by OCT, which, in the investigator's opinion, contributes to the macular edema, or causes associated foveal detachment, and would preclude improvement with pegaptanib sodium.
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Previous treatment with intravitreal corticosteroids in the study eye within 3 months of Day 0 visit.
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Previous treatment with intravitreal anti-angiogenic drugs in the study eye within 2 months of Day 0 visit.
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Previous intraocular surgery within 30 days of Day 0 visit.
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Any ocular or periocular infection within 30 days of Day 0 visit.
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Any of the following underlying diseases including:
History or evidence of severe cardiac disease (e.g., NYHA Functional Class III or IV - see Appendix 16.6), clinical or medical history of unstable angina, acute coronary syndrome, myocardial infarction or revascularization within 6 months, ventricular tachyarrythmias requiring ongoing treatment.
History or evidence of clinically significant peripheral vascular disease, such as intermittent claudication or prior amputation.
History or evidence of clinically significant impaired renal or hepatic function Stroke (within 12 months of trial entry). Any major surgical procedure within one month of trial entry.
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Any treatment with an investigational agent in the past 30 days for any condition.
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Known serious allergies to the fluorescein dye used in angiography or to the components of pegaptanib sodium formulation.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Retina Institute of Hawaii | Honolulu | Hawaii | United States | 96815 |
Sponsors and Collaborators
- Retina Institute of Hawaii
- Eyetech Pharmaceuticals
Investigators
- Principal Investigator: Michael D Bennett, MD, Retina Institute of Hawaii
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- RIH 1006