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Arteriovenous Fistula clinical trials

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NCT ID: NCT00912782 Completed - Clinical trials for End-stage Renal Disease

Vitamin D and Arteriovenous Fistulae

Start date: January 2009
Phase: N/A
Study type: Interventional

Patients requiring hemodialysis following kidney failure need a form of dialysis vascular access in order to undergo the dialysis procedure. Dialysis vascular access dysfunction is an enormous clinical problem. While the best form of vascular access is the arteriovenous fistula (AVF), its primary problem is early, aggressive cellular ingrowth that leads to poor maturation of the vessel, preventing its use for dialysis. Strategies to prevent AVF failure are needed. Vitamin D is a hormone present in all human bodies and is important for good bone formation and immune function. There is new information that links vitamin D to the function of our veins and arteries, which are used in the creation of an arteriovenous fistulae. Our bodies can make vitamin D and can also get vitamin D from our diet. However, a majority of patients with chronic kidney disease and end-stage renal disease (ESRD) have low vitamin D levels (vitamin D deficiency). There are several benefits to correcting low vitamin D levels, however, it is not know whether correcting low vitamin D in the body will lead to better function of the vein and artery used for arteriovenous fistulae creation. The main goal of this pilot study is to examine the role of vitamin D supplementation on AVF maturation and useability for dialysis. Study results will be used to develop larger studies to examine the specific effect that vitamin D supplementation has on the vessels used for AVF creation and whether vitamin D promotes AVF maturation.

NCT ID: NCT00840372 Completed - Clinical trials for Chronic Hemodialysis Patients

Semi-blunt Needles: is Outcome Better?

Needles
Start date: November 2008
Phase: N/A
Study type: Observational

The aim of this observational study in patients chronically hemodialyzed by a native arterio-venous fistula is to determine the impact of the use of semi-blunt needles on the quality of the punction. The investigators have observed that cannulation with blunt needles (button-hole method) is sometimes difficult and the use of a sharp needle may be necessary, with consequently more hematomes and infections. Our hypothesis is that canulation with semi-blunt needles would be easier than with classical blunt needles, and consequently the use of sharp needles would become less frequent. Inclusion criteria and study design are detailed below.

NCT ID: NCT00836862 Completed - Clinical trials for Kidney Failure, Chronic

Arteriovenous Fistula Tissue Bank for Pre- and Post-Fistula Placement Specimens

Start date: February 1, 2009
Phase:
Study type: Observational

This project will bank sera, DNA and vascular specimens from patients undergoing arteriovenous fistula creation and revision.

NCT ID: NCT00733759 Withdrawn - Clinical trials for Pulmonary Arteriovenous Malformations

Contrast Echocardiography in Patients With Pulmonary Arteriovenous Malformations (PAVMs)

Start date: February 2004
Phase:
Study type: Observational

Pulmonary arteriovenous malformations (PAVMs) are thin-walled abnormal vessels which provide direct capillary-free communications between the pulmonary and systemic circulations. Patients with PAVMs have usually have low blood oxygen levels and are at risk of other complications including strokes, brain abscesses, pregnancy-related complications and haemorrhage. We hypothesise that the complications of PAVM patients arise from their PAVMs and not the more recognised intracardiac forms of shunting. We propose to perform echocardiograms to enable assessment of the presence of other causes of capillary-free communications between the pulmonary and systemic circulations.

NCT ID: NCT00679991 Completed - Clinical trials for Chronic Kidney Disease

A Phase 1-2 Study of PRT-201 Administered in Chronic Kidney Disease (CKD) Patients

Start date: November 2008
Phase: Phase 1/Phase 2
Study type: Interventional

PRT-201 is a protein that causes long lasting dilation of blood vessels when applied to the outside surface of the blood vessel. The purpose of this study is to determine if PRT-201, when applied to a limited segment of blood vessel immediately after surgery to create an arteriovenous fistula (AVF), is safe, dilates the blood vessel, and increases blood flow through the AVF.

NCT ID: NCT00602004 Completed - Renal Failure Clinical Trials

Attenuation of Cardiac Effects of Arteriovenous Fistula Creation With Losartan

Start date: October 2006
Phase: N/A
Study type: Interventional

The primary objective is to determine if the use of losartan, an angiotensin II receptor blocker, can attenuate left ventricular hypertrophy, independent of its antihypertensive effects, in patients with near end stage chronic kidney disease (CKD) who have an arteriovenous fistula created. Secondary outcomes include the impact of the medication on BNP and hyperkalaemia

NCT ID: NCT00543348 Withdrawn - Stenosis Clinical Trials

RCT of the Cutting Balloon Versus a High Pressure Balloon for the Treatment of Arteriovenous Fistula Stenoses

Start date: September 2007
Phase: N/A
Study type: Interventional

The proposed study will investigate the efficacy of the peripheral cutting balloon (PBC) compared to the high pressure balloon in dilating venous stenosis in hemodialysis fistulas. 2. SPECIFIC AIMS Study endpoints will be: Primary Endpoint 1. Primary and assisted patency at 6 months Secondary Endpoints: 1. Procedure effectiveness/residual stenosis 2. Procedure-related complications 3. Primary patency and primary assisted patency 12 months 4. Secondary patency at 6 and 12 months 5. Number/type of secondary interventions.

NCT ID: NCT00522704 Recruiting - Clinical trials for Arteriovenous Fistula

Correlation Between Access Blood Flow and Extracorporeal Blood Flow

Start date: March 2008
Phase: N/A
Study type: Observational

The purpose of this study is to determine if Effective Extracorporeal Blood Flow(eEBF) has correlation with Access Blood Flow (Qa), when eEBF adjusts with Dynamic Arterial Line Pressure (DALP) in patients with Arteriovenous fistulae in hemodialysis treatment.

NCT ID: NCT00368147 Completed - Clinical trials for Arteriovenous Fistula

Access Creation for Hemodialysis: Association With Structural Changes of the Heart

Start date: April 2002
Phase:
Study type: Observational

The purpose of this study is to determine if the creation of a fistula or a graft plays a role in the development of heart disease for patients undergoing hemodialysis

NCT ID: NCT00001364 Completed - Clinical trials for Arteriovenous Fistula

Evaluation and Treatment of Patients Spinal Blood Vessel Abnormalities

Start date: June 2, 1993
Phase: N/A
Study type: Observational

Arteriovenous malformations (AVM) are abnormally formed blood vessels that can be located throughout the brain and spinal cord. Patients with abnormalities of the blood vessels located in and around the spinal cord can develop many neurological problems. Some problems include, weakness, pain, difficulty walking, paralysis, and even death. The treatment for these AVMs depends on their location, the type of malformation, the area of the spine involved, and the condition of the patient at the time of treatment. The treatment is aimed at stopping the neurologic problems from worsening and possibly correcting the existing problems. There are two commonly used treatments for AVMs, surgery and embolization (blocking off of blood flow to the AVM). However, researchers have limited experience treating these conditions because they are rare. In addition, it has been difficult to classify different kinds of AVMs and to develop new treatments for them. This study is designed to increase researchers understanding of AVMs by admitting and following patients diagnosed with the condition. By increasing the amount of patients studied diagnosed with spinal blood vessel abnormalities, researchers can begin to develop new management plans for patients with AVMs.