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Volume Flow-guided Angioplasty of Dysfunctional Dialysis Access

NCT04430478 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2020-12-22

No results posted yet for this study

Summary

This is a pilot study investigating a new concept of intra-procedural percutaneous duplex ultrasound (DUS) volume flow-guided balloon angioplasty for the quantification and optimization of endovascular treatment outcomes of dysfunctional autologous arteriovenous fistulae (AVF).

Conditions

  • Dialysis Access Malfunction

Interventions

DIAGNOSTIC_TEST

Volume flow guided angioplasty

Volume flow measurements using DUS will be obtained at the end of each balloon dilation, at 24 hours, 6 months, and one year after index procedure.

Sponsors & Collaborators

  • Attikon Hospital

    lead OTHER

Principal Investigators

  • Stavros Spiliopoulos, MD, PhD, EBIR · ATTIKO University Hospital

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-06-10
Primary Completion
2020-12-21
Completion
2020-12-21

Countries

  • Greece

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04430478 on ClinicalTrials.gov