Propranolol for Diabetic Retinopathy



Status:Completed
Conditions:Ocular, Diabetes
Therapuetic Areas:Endocrinology, Ophthalmology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:February 2012
End Date:December 2015

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This study is investigating if the oral beta antagonist propranolol can induce regression of
retinal neovascularization associated with proliferative diabetic retinopathy.

Oral propranolol 120mg daily will be given to 10 patients with proliferative diabetic
retinopathy over a 12 week period to evaluate the effect on retinal neovascularization.

Inclusion Criteria:

- Age >=18 years

- Eyes with proliferative diabetic retinopathy and neovascularization

- Eyes with a history of panretinal photocoagulation treatment and persistent
neovascularization deemed by the investigator to be a potential threat to visual
acuity either by causing a vitreous hemorrhage or tractional retinal detachment.
(Group 1 - maximum 5 eyes enrolled with these characteristics)

- Eyes without a history of panretinal photocoagulation treatment, but that do not have
high-risk proliferative diabetic retinopathy characteristics (i.e. these are eyes
that have early proliferative diabetic retinopathy that are not yet at a high-risk
for vitreous hemorrhage and tractional retinal detachment such that panretinal
photocoagulation laser may be deferred). (Group 2 - maximum 5 eyes enrolled with
these characteristics)

Exclusion Criteria:

- Either panretinal photocoagulation laser or focal/grid laser into study eye within 3
months of study enrollment

- Anti-Vascular endothelial growth factor injection into study eye within 3 months of
study enrollment

- Contraindications to beta-blockers such as: allergy, previous intolerance, abnormally
slow heart rates, asthma or chronic obstructive pulmonary disease, use of medications
that have an effect on certain drug metabolic pathways that may cause interactions.

- Known coronary arterial disease or left ventricular dysfunction, or known peripheral
vascular disease

- Resting heart rate <60 or systolic blood pressure <90 and/or diastolic blood pressure
<50

- Pregnancy

- All patients will either be post-menopausal, have adequate birth control and, if of
childbearing age, will have a urinary pregnancy test performed

- Allergy to fluorescein dye

- Media opacity obscuring adequate determination of neovascularization including dense
cataract or dense vitreous hemorrhage

- Patient is already taking an oral beta-blocker

- Vulnerable populations such as prisoners and minors will also be excluded
We found this trial at
1
site
Madison, Wisconsin 53706
(608) 263-2400
University of Wisconsin-Madison In achievement and prestige, the University of Wisconsin-Madison has long been recognized...
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Madison, WI
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