Phase
Condition
Intermittent Claudication
Vascular Diseases
Peripheral Arterial Occlusive Disease
Treatment
L-Ascorbate
Tetrahydrobiopterin 10 mg/kg
Tetrahydrobiopterin 20 mg/kg
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
PAD as demonstrated by an ABI <0 .9 in one leg or TBI less than <0.7 in patientswith an ABI >1.3 (non compressible vessels)
Rutherford Classification II, III
Age >18 years old
Willingness to discontinue phosphodiesterase (PDE) 5 inhibitors such as Viagra,Cialis, Levitra, Revatio
Willingness to discontinue phosphodiesterase (PDE) 3inhibitors cilostazol, milrinoneor Vesnarinone
Willing and able to comply with all study procedures
Willing and able to provide informed consent
Sexually active subjects willing to use an acceptable method of contraception whileparticipating in the study
Exclusion
Exclusion Criteria:
Hypotension defined as a systolic blood pressure less than 100mmhg systolic atscreening or baseline visit
Critical Leg Ischemia (Rutherford Classification IV, V, VI)
Surgical intervention to alleviate symptoms of claudication in the study leg withinthe past 6 months or any endovascular interventions within 3 months or who isscheduled to undergo surgical revascularization in the next 6 month
Walking limited by reasons other than claudication (e.g. arthritis, lung disease,severe neuropathy, lower extremity amputation except single digits)
Serum creatinine >1.5mg/dl or Hepatic enzymes >2X the upper limit of normal
Serum potassium greater than 5.0 or use of a potassium sparing diuretic at screening
Pregnant, breast feeding or planning to become pregnant (subject or partner) at anytime during the study.
Myocardial Infarction, Cerebrovascular Accident or deep vein thrombosis within 12months of screening
Known history of nephrolithiasis
History of ever having a seizure
Concurrent disease or condition that would interfere with study participation orsafety such as bleeding disorders, organ transplant, long term immunosuppression (excluding inhaled steroids), current neoplasm or severe gastroesophageal reflux
History of vertigo or syncope within the past 10 years
Enrollment in another drug or device study within 30 days of screening
Required treatment with a drug known to inhibit folate metabolism (e.g.Methotrexate)
Taking any of the following medications; PDE3 Inhibitors, PDE5 inhibitors, trental,nitrates, ginkgo biloba, levodopa, warfarin,
Axillary lymph node dissection
Presence of an amputation except single digits in either leg
Preexisting illness that limits ambulation such as severe COPD, class III-IV heartfailure, severe arthritis or back pain
Glucose-6-dehydrogenase deficiency
Study Design
Study Description
Connect with a study center
UMASS Memorial Healthcare - University Campus
Worcester, Massachusetts 01655
United StatesActive - Recruiting
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