Atherosclerotic Renal Artery Stenosis Clinical Trial
• Background: Since evidence show that renal-artery stenting did not confer a significant
benefit with respect to the prevention of clinical events when added to comprehensive,
multifactorial medical therapy in people with atherosclerotic renal-artery stenosis[1], the
aim of our study was to confirm Fu-zheng-qu-zhuo (FZQZc) oral liquid, a herbal medicine,
combined with optimal medical therapy of internal medicine (OMT), including anti-platelet
therapy and other protocol-driven medical therapies to control blood pressure and glucose
and lipid levels in accordance with guidelines,resulted in greater renal function protection
in patients with atherosclerotic renal artery stenosis ( ARAS) compared with OMT alone.
Methods : A randomized, placebo-controlled, single centre clinical design. Sixty patients
with diagnosed atherosclerotic renal artery stenosis and had chronic kidney disease stage 3
will be recruited, and will be randomized into two groups in a 1:1 ratio ( FZQZ and placebo
Group, 30 respectively). FZQZ Oral liquid or placebo 20 ml every time, three times a day for
different groups, meanwhile, all participants in both treatment groups received OMT, 6
months therapeutic period. Serum creatinine, estimated glomerular filtration rate(eGFR),
urine protein, and cardiovascular and renal events (a composite end point of death from
cardiovascular or renal causes, myocardial infarction, stroke, hospitalization for
congestive heart failure, progressive renal insufficiency, or the need for renal-replacement
therapy) will be compared between the Groups as the outcome.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | |
Est. primary completion date | September 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: 1. Met the ARAS diagnosis: renal angiography or magnetic resonance angiography (MRA) shows renal artery with unilateral or bilateral stenosis at least 50%,and with artery atheromatous plague; 2. Meeting with the diagnostic criteria of the K/DOQI chronic kidney disease (eGFR<90ml/min):light or moderate damage to kidney function,Scr<265.2µmol/L(3.0mg/dl). Exclusion Criteria: 1. Patients with renal artery stenosis which had been suspected or final diagnosed to be Fibromuscular dysplasia or Takayasu arteritis; 2. Blood pressure did not meet the target (<140/90mmHg) after combinedly taking more three kinds of antihypertensive agents with maximum dose; 3. Poor control of blood sugar in patients with Diabetes ( glycosylated hemoglobin 8.0% or higher in the recent month); 4. History of peptic ulcer,with Gastrointestinal bleeding in the recent 6 months; 5. decompensated cirrhosis; 6. Hematologic disease or bleeding tendency; 7. Repeated episodes of pulmonary edema, congestive heart failure, acute myocardial infarction, cerebral infarction and cerebral hemorrhage in recent 3 months; 8. Suffering from malignant tumor and predicting life span less than 1 year. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
China | Guang anmen Hospital,China Academy of Chinese Medical Sciences | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
Guang'anmen Hospital of China Academy of Chinese Medical Sciences |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | urine protein | six month | No | |
Primary | estimated glomerular filtration rate filtration rate | the change of eGFR during the observation period | six month | No |
Secondary | cardiovascular and renal events (a composite end point of death from cardiovascular or renal causes( myocardial infarction, stroke, hospitalization for congestive heart failure, progressive renal insufficiency, or the need for renal-replacement therapy) | six month | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01840540 -
MSC for Occlusive Disease of the Kidney
|
Phase 1 |