Status:
UNKNOWN
Efficacy Study of Oral L-Citrulline in Patients Taking Simvastatin With Peripheral Arterial Disease
Lead Sponsor:
Angiogenix
Conditions:
Peripheral Arterial Disease
Intermittent Claudication
Eligibility:
All Genders
40-75 years
Phase:
PHASE2
Brief Summary
To prove the combination of L-citrulline with simvastatin leads to greater improvement in the symptoms of peripheral arterial disease (PAD) than simvastatin alone by evaluating oral L- citrulline or p...
Detailed Description
The primary objective of this study is to prove the combination of L-citrulline with simvastatin leads to greater improvement in the symptoms of PAD than simvastatin alone. This will be accomplished b...
Eligibility Criteria
Inclusion
- Male or female, 40-75 years of age
- If female, post-menopausal for the past year, surgically sterile (i.e., tubal ligation, hysterectomy), or using an adequate method of birth control (i.e., oral contraceptives, double barrier method, IUD cover, sterilized partner, or other method deemed appropriate by Investigator)
- If male capable of fathering children, using an adequate method of birth control (i.e., condom or partner using adequate method of birth control)
- Peripheral arterial disease with stable, reproducible, intermittent claudication and symptom-limited treadmill walking distance of at least 6 months duration
- Rest ankle-brachial index (ABI) ≤0.90 and 10 mm Hg decrease in ankle pressure 1 minute after completing the ETT
- ACWD on a standardized (Skinner-Gardner protocol) ETT ≥50 m (164 feet) but ≤300 m (984 feet) determined by the average result on two consecutive ETTs performed at least 7 days apart during the screening phase (Fontaine stage II)
- ACWD variability \<25% between two consecutive ETTs performed at least 7 days apart during the screening phase. The percent variability is calculated by the difference of the two walking distances divided by the greater of the two walking distances multiplied by 100%. If the variability exceeds 25% a third ETT may be performed and the variability between the second and third test used to determine baseline and inclusion criteria
- Willingness to receive dietary counseling and follow a low-cholesterol diet during the study
- Ability to give written informed consent and has signed a written informed consent form approved by the Investigator's Independent Ethics Committee (IEC)
Exclusion
- Critical limb ischemia (defined as presence of rest pain requiring analgesics for more than 2 weeks or the presence of lower limb ulcers or gangrene)
- Coronary artery or peripheral artery angioplasty or surgical limb arterial bypass within the last 3 months
- Any previous amputation on the lower limbs
- Anticipated requirement of surgical or percutaneous revascularization within 3 months of randomization
- Currently participating in a supervised exercise regimen
- Stroke, myocardial infarction, or deep-vein thrombosis within the last 3 months
- Non-atherosclerotic PAD (e.g., thromboangiitis obliterans)
- Known abdominal aortic aneurysm ≥4.5 cm
- Unstable angina pectoris within the last 3 months
- Congestive heart failure (New York Heart Association Class III or IV) despite treatment
- Severe, uncontrolled hypertension (sitting systolic blood pressure \>180 mm Hg or sitting diastolic blood pressure \>95 mm Hg)
- Anemia (hemoglobin \<10 g/dL in women and 11 g/dL in men) or any clinically significant bleeding episode within the last year
- Abnormal platelet count (platelets \>150,000/mm3 or \<60,000/mm3)
- Type I diabetes mellitus or Type II diabetes mellitus if it is accompanied by diabetic peripheral neuropathy
- Morbid obesity (body mass index \>40 kg/m2)
- Severe renal insufficiency (creatinine \>221 µmol/L (2.5 mg/dL))
- Severe hepatic insufficiency (ALT \[SGPT\] and AST \[SGOT\] ≥ 3x upper limit of normal on two separate tests
- Any disorder that would affect the interpretation of ETT results
- Use of medications that are not allowed and which cannot be discontinued during the study
- Participation in an investigational drug or device study within previous 30 days
- Underlying disease other than PAD resulting in a life expectancy of less than 1 year
- If female, breast feeding, pregnancy confirmed by a positive serum pregnancy test, or using inadequate birth control
- Other conditions that could impair informed consent or compliance
Key Trial Info
Start Date :
March 1 2006
Trial Type :
INTERVENTIONAL
End Date :
Estimated Enrollment :
160 Patients enrolled
Trial Details
Trial ID
NCT00351286
Start Date
March 1 2006
Last Update
October 18 2006
Active Locations (10)
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1
Municipal Healthcare Institution, Gatchina Central District Hospital
Gatchina, Russia, Russia, 188300
2
Russian State Medical University at Filatov City Hospital #15
Moscow, Russia, Russia, 111539
3
Vishnevsky Institute of Surgery, Russian Medical Academy of Science
Moscow, Russia, Russia, 113811
4
Municipal Prophylaxis and Treatment Institution, City Hospital #13
Nizhny Novgorod, Russia, Russia, 603018