Kidney Disease Clinical Trial
Official title:
Evidence of Procedural Embolism Complicating Renal Artery Stenting
This study will use magnetic resonance imaging (MRI) to picture the kidney and renal
arteries (arteries that supply blood to the kidney) in patients scheduled for kidney artery
angiogram and angioplasty/stenting procedures. An angiogram is a way of taking pictures of
arteries that shows areas of narrowing caused by atherosclerosis-a buildup of plaque on the
vessel wall. Angioplasty/stent is a treatment procedure in which a balloon-tipped catheter
is inserted in the artery and advanced to the area of blockage to open the vessel,
increasing blood flow to the kidney. A permanent metal tube (stent) may or may not be put in
place to maintain the opening. During either of these invasive procedures, small pieces of
plaque can break off and travel in the blood to lodge elsewhere in the body. This is called
embolization. Lodged in the kidney, the embolus can impair kidney function. Currently, these
emboli cannot be detected. A new way of visualizing the kidneys that allows detection of
emboli may reveal whether material has moved to the kidneys and predict if there will be any
kidney damage.
Patients 21 years of age and older with suspected kidney artery disease scheduled for
invasive angiographic evaluation in NIH protocol 95-H-0047 may be eligible for this study.
Participants will be assigned to one of two study groups, based on the angiogram findings
and the decision to have the angioplasty/stent procedure. Participants in both groups will
have baseline MRI scans up to 2 weeks before the invasive procedure (angiogram with or
without angioplasty/stent) and again within a day after the procedure. Patients who undergo
angioplasty/stent will have another MRI study within about a month following the procedure.
MRI uses a magnetic field and radio waves to produce images of body tissues. The patient
lies on a table that slides into a large hollow tube (the scanner). During part of the scan,
a material called gadolinium contrast may be injected into a vein. This substance brightens
the images to better show the kidneys, their blood vessels and blood flow. The procedure
lasts from about 1 to 2 hours. During the MRI, the heart is monitored with an
electrocardiogram (EKG) and breathing is monitored with a flexible belt. Blood pressure is
measured intermittently. The patient can communicate with a staff member at all times.
Blood samples will be drawn from an arm vein at the initial clinic visit, within a day after
the procedure and about 1 week after the procedure. For patients who had the
angioplasty/stent procedure, a third blood sample will be taken within another 6 six weeks.
The blood samples will be used to check for changes in kidney function.
Status | Completed |
Enrollment | 60 |
Est. completion date | December 2005 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
INCLUSION CRITERIA: Adult patients with clinically suspected renovascular disease undergoing invasive angiographic assessment in protocol 95-H-0047 at the NIH CC. Adult patients with clinically suspected renovascular disease undergoing invasive angiographic assessment at other medical centers. EXCLUSION CRITERIA - Contraindications to MRI: Cardiac pacemaker or implantable defibrillator Cerebral aneurysm clip Neural stimulator (e.g. TENS-Unit) Any type of ear implant Metal in eye (e.g. from machining) Any implanted device (e.g. insulin pump, drug infusion device) Known hypersensitivity to gadolinium contrast agents EXCLUSION CRITERIA - General: Patients less than 21 years old Pregnant or lactating women |
Endpoint Classification: Safety Study, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | National Heart, Lung and Blood Institute (NHLBI) | Bethesda | Maryland |
Lead Sponsor | Collaborator |
---|---|
National Heart, Lung, and Blood Institute (NHLBI) |
United States,
Conlon PJ, O'Riordan E, Kalra PA. New insights into the epidemiologic and clinical manifestations of atherosclerotic renovascular disease. Am J Kidney Dis. 2000 Apr;35(4):573-87. Review. — View Citation
Harden PN, MacLeod MJ, Rodger RS, Baxter GM, Connell JM, Dominiczak AF, Junor BJ, Briggs JD, Moss JG. Effect of renal-artery stenting on progression of renovascular renal failure. Lancet. 1997 Apr 19;349(9059):1133-6. — View Citation
Textor SC, Wilcox CS. Renal artery stenosis: a common, treatable cause of renal failure? Annu Rev Med. 2001;52:421-42. Review. — View Citation
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02369354 -
Transplant Social Worker Support for Live Kidney Donation in African Americans
|
N/A | |
Not yet recruiting |
NCT02225782 -
Trial to Compare 1.0 Versus 2.0 mg Alteplase (tPA) Dosing in Restoring Hemodialysis Catheter Function
|
Phase 4 | |
Completed |
NCT00499187 -
Fanconi Syndrome Due to ARVs in HIV-Infected Persons
|
Phase 4 | |
Withdrawn |
NCT00585429 -
Evaluation of Kidney Disease in Liver Transplant Recipients
|
N/A | |
Completed |
NCT00379899 -
ADVANCE: Study to Evaluate Cinacalcet Plus Low Dose Vitamin D on Vascular Calcification in Subjects With Chronic Kidney Disease Receiving Hemodialysis
|
Phase 4 | |
Completed |
NCT00183248 -
Using Donor Stem Cells and Alemtuzumab to Prevent Organ Rejection in Kidney Transplant Patients
|
Phase 1/Phase 2 | |
Completed |
NCT00001835 -
Oxaliplatin in Cancer Patients With Impaired Kidney Function
|
Phase 1 | |
Completed |
NCT01331941 -
A Pharmacokinetic Study of AMG 386 in Cancer Subjects With Normal and Impaired Renal Function
|
Phase 1 | |
Terminated |
NCT00436748 -
Study to Assess Darbepoetin Alfa Dosing for the Correction of Anemia in Pediatric Patients With Chronic Kidney Disease
|
Phase 3 | |
Completed |
NCT01467466 -
Prevention of Serious Adverse Events Following Angiography
|
Phase 3 | |
Completed |
NCT01235936 -
Safety and Efficacy Study for AKB-6548 in Participants With Chronic Kidney Disease and Anemia
|
Phase 2 | |
Completed |
NCT01947829 -
Interdialytic Kt/V Variability Measurement With Adimea (IVP STUDY)
|
N/A | |
Completed |
NCT01974999 -
A Retrospective Multicenter Study to Determine 5-Year Clinical Outcomes in Subjects Previously Enrolled in the CTOT-01 Study
|
||
Recruiting |
NCT01240564 -
The Nephrotic Syndrome Study Network (NEPTUNE)
|
N/A | |
Active, not recruiting |
NCT01228903 -
Uric Acid and the Endothelium is CKD
|
N/A | |
Completed |
NCT00734357 -
Comparative Investigation of Intravenously Administered Omnipaque and Isovue: Effects on Serum Creatinine Concentration in Outpatients
|
N/A | |
Completed |
NCT00781417 -
Prevention of Secondary Hyperparathyroidism With Vitamin D in Stage II/III Chronic Kidney Disease
|
N/A | |
Completed |
NCT00094484 -
Cinacalcet HCl in Chronic Kidney Disease Subjects With Secondary Hyperparathyroidism Not Receiving Dialysis
|
Phase 3 | |
Completed |
NCT00185159 -
Olmesartan Medoxomil in Diabetes Mellitus
|
Phase 3 | |
Completed |
NCT00093977 -
Study to Assess Darbepoetin Alfa in Subjects With Chronic Kidney Disease
|
Phase 3 |