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Trial Comparing Angiography and Angiography With IVUS for Treatment of Hemodialysis Access Failures

A Prospective Randomized Feasibility Trial Comparing Angiography and Angiography With IVUS for Treatment of Hemodialysis Access Failures

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02056704
Enrollment
66
Registered
2014-02-06
Start date
2014-02-18
Completion date
2022-02-01
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dialysis Access Malfunction

Keywords

Dialysis Fistula, Dialysis Graft, Stenosis, Intravascular Ultrasound, Angiography

Brief summary

The reason the investigators are doing this study is to compare the results of angiography versus angiography with intravascular ultrasound in dialysis grafts/fistulas that are blocked.

Detailed description

Patients with kidney failure have a fistula or graft for long-term dialysis in order for the dialysis machine to draw blood, filter it, and give it back to the patient. Over time, the fistula or graft may not work well enough to use for dialysis, most commonly because the veins may develop "scar tissue" within and around them that narrows the vein resulting in poor flow or complete blockage. These blockages are commonly opened with wires, balloons (a procedure called angioplasty), and stents. These blockages are seen with angiography, a special type of x-ray used with a dye that shows the inside of the blood vessels. Intravascular ultrasound (IVUS) is a type of imaging that uses sound waves to produce an image of the inside of blood vessels and to see their condition. Currently, it is not known if angiography alone or angiography with IVUS has better results. The reason we are doing this study is to compare the results of angiography versus angiography with IVUS.

Interventions

DEVICEAngiography with IVUS

The use of IVUS to evaluate dialysis access failure.

Sponsors

Baylor Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* \> 18 years old * Male or female (non-pregnant females) * Patients with hemodialysis access failure (arteriovenous fistulae or arteriovenous grafts) * Patients must undergo elective angiographies (fistulograms) based on surveillance duplex ultrasound findings (stenosis) * Patients with outflow stenoses between 1 cm distal to an arterial anastamosis and clavicle in AV fistulae or between venous anastamosis and clavicle in AV grafts found on surveillance duplex ultrasound

Exclusion criteria

* Patients with other etiologies (inflow lesions, intragraft lesions, hypercoagulable states, lesions not readily amenable to stenting), advanced failures (thrombosis, central venous occlusion), and non-routine access conformations (chest wall/groin grafts, balloon assisted maturation)

Design outcomes

Primary

MeasureTime frameDescription
Change in characteristics of lesion within the vesselevery 3 months - up to 2 yearsThis will include vessel diameters proximal and distal to lesions, percent stenosis, and lesion lengths.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORWilliam Shutze, MD

Baylor Health Care System

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026