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Arteriovenous Fistula clinical trials

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NCT ID: NCT03189667 Terminated - Clinical trials for Dysfunctional Dialysis Arteriovenous Fistula

Drug Coated Balloons vs Plain Balloons for the Management of Dysfunctional Dialysis Fistula

Start date: October 15, 2017
Phase: N/A
Study type: Interventional

Compare the effectiveness of drug-coated balloons to plain balloon angioplasty in reducing stenosis rates in dialysis arteriovenous fistulas (AVFs).

NCT ID: NCT03188978 Withdrawn - Clinical trials for Primary Arteriovenous Fistula Failure

High-intensity Atorvastatin for Arteriovenous Fistula Failure (HAFF): A Feasibility Pilot Study

HAFF
Start date: November 1, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

Primary failure is the most common complication of newly created arteriovenous fistulas (AVFs) and an important contributor to end stage renal disease (ESRD) patients' morbidity and mortality. Recently, the investigators have found that high intensity atorvastatin (40 mg/day) reduces AVF primary failure significantly when compared to other statins or no statin treatment in three separate prospective and retrospective studies done in collaboration with the University of Miami. Based on these findings and considering the necessity for a therapy to improve AVF maturation rates, the investigators propose the realization of a feasibility pilot double blinded randomized controlled trial (RCT). In this study, a total of 50 patients will be randomly allocated to receive high intensity atorvastatin (40 mg daily) or placebo starting at two weeks before surgery and until the end of the observational period (6 weeks after surgery). Present trial will reveal crucial feasibility information such as the appropriateness of the eligibility criteria, patient recruitment and retention rates, compliance, adverse events, efficacy of patient follow-ups, and readiness of the facilities and involved personnel; while having as a secondary endpoint the predictive measurements of diameter and AVF blood flow 6 weeks after fistula creation useful for the estimation of the probable effect of proposed intervention. Here, the investigators aim to pave the way for a future multicenter Phase II RCT seeking to prove the efficacy of atorvastatin therapy as a perioperative intervention to reduce AVF primary failure.

NCT ID: NCT03171701 Not yet recruiting - Clinical trials for Arteriovenous Fistula

Color Doppler Ultrasonography in Prediction of Arteriovenous Fistula Maturation in Hemodialysis Patients

Start date: July 1, 2017
Phase: N/A
Study type: Observational

The transplant is the definitive treatment of renal insufficiency, in our days. While waiting for it, the arteriovenous fistula surgery is standard procedure.

NCT ID: NCT03142360 Recruiting - Clinical trials for Arteriovenous Fistula Patency

Effect of Beraprost Sodium (Berasil) on Hemodialysis

Start date: April 5, 2017
Phase: N/A
Study type: Interventional

There is no randomized control study to determine if the beneficial effects of beraprost sodium could improve the patency of arteriovenous fistula in hemodialysis patients. Therefore, this study is aimed to demonstrate the use of beraprost sodium can improve the patency of arteriovenous fistula in patients undergoing hemodialysis. This study is prospectively randomize controlled open-label trials in patients who newly made artificial arteriovenous fistula for hemodialysis. This study is a pilot study, and the target number of subjects is 60 in total, 30 in the treatment group and 30 in the control group. After randomization, the treatment group takes a beraprost sodium for 6 months and the control group does not take placebo. Treatment lasts for 6 months after dosing but continues until the patient changes the renal-replacement therapy method or falls under the exclusion criteria. The patient should visit at 1, 3, and 6 months after arteriovenous graft surgery to check the access site after graft surgery. The doppler ultrasound test is performed to measure the access blood flow rate and patency of arteriovenous fistula.

NCT ID: NCT03137680 Not yet recruiting - Clinical trials for Arteriovenous Fistula

Pre-Operative Forearm Exercise On Arteriovenous Fistula Mauration

Start date: May 15, 2017
Phase: N/A
Study type: Interventional

To investigate the effect of pre-operative exercise on 1. Hemodynamics in the fistula artery and vein, pre and post AV fistula formation 2. Suitability of cannulation of AV fistula at 8weeks

NCT ID: NCT03106948 Recruiting - Clinical trials for Arteriovenous Fistula Occlusion

Delivery of Inhibitors of Lysyl Oxidase (LysoLox) on Serial Angioplasty and Time to Restenosis

Start date: February 1, 2017
Phase: Phase 2
Study type: Interventional

The narrowing of Dialysis Fistulae or Grafts is a near universal problem in patients with end-stage renal disease (ESRD) and requires patients to undergo repeated angioplasty or mechanical opening of the fistula.

NCT ID: NCT03077815 Completed - Clinical trials for Systematically Intermittent Arm Exercise for Improving Maturation of Hemodialysis Arteriovenous Shunt

Systematically Intermittent Arm Exercise for Improving Maturation of Hemodialysis Arteriovenous Shunt: Study Protocol for a Randomized Controlled Trial

Start date: April 1, 2017
Phase: N/A
Study type: Interventional

Arm vein intermittently gripping arm movements, can promote the increased diameter of arteriovenous fistula, which enhance the maturity of fistula, the effect of lack of empirical research. Objective: this study, randomized controlled study, investigate systematic random arm vein pressure and arm movements to arteriovenous fistula in hemodialysis patients improve the maturity rate and effectiveness of the diameter. Methods: a prospective comparative study randomly assigned.

NCT ID: NCT03068845 Not yet recruiting - Clinical trials for Stenosis of Arteriovenous Dialysis Fistula

Arteriovenous Fistula: Conventional Angioplasty vs Drug Eluting Balloon-assisted Maturation Intervention Clinical Trial

ACADEMIC
Start date: June 2017
Phase: Phase 3
Study type: Interventional

The purpose of this randomised clinical trial is to evaluate the efficacy of drug-eluting balloon compared to conventional balloon in balloon-assisted maturation of non-maturing arteriovenous fistula in adult renal failure patients.

NCT ID: NCT03054623 Recruiting - Clinical trials for Chronic Kidney Diseases

Hemodynamic Assessment of Distal Revascularization Interval Ligation

DRIL
Start date: September 20, 2016
Phase: N/A
Study type: Observational

Our study seeks to define the effect of each component of the distal revascularization interval ligation (DRIL) procedure on the in vivo distal blood pressure of patients with ischemic steal, and to determine whether the interval ligation component of the DRIL procedure is necessary or not.

NCT ID: NCT03044496 Completed - Clinical trials for Arterio-venous Fistula

NIRS Measurement After SCP Block

Start date: September 2016
Phase:
Study type: Observational

Peripheral regional anesthesia induces a sympathectomy-like effect with neurovascular changes causing increased arterial blood flow and venodilatation . Near-infrared spectroscopy (NIRS) can be applied to different kinds of tissue providing oxygen saturation by detecting the absorption and reflection of near-infrared light . The effect on peripheral tissue oxygenation in patients undergoing arteriovenous fistula revision has not yet been examined. We postulate an increase in tissue oxygenation by sympathicolysis caused by peripheral regional anesthesia that might be the reason for beneficial outcome. The aim of our study was to demonstrate the effect of a supraclavicular plexus block in this group of patients.