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Guided Needle Insertion for Vascular Access

NCT07548151 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2026-05-29

No results posted yet for this study

Summary

The goal of this clinical trial is to determine whether the study device can assist the cannulator with placing two needles during cannulation required to initiate dialysis treatment.

Males or females with end-stage kidney disease who are 18 and older and not pregnant or breastfeeding can be included in the study.

The main question it aims to answer is:

Can the study device guide the cannulator to the arteriovenous fistula (AVF) or arteriovenous graft (AVG) and assist the cannulator with needle insertion into the AVF or AVG for dialysis cannulation?

Conditions

  • End Stage Renal Failure, Hemodialysis
  • Cannulation

Interventions

DEVICE

Ultrasound-Guided, Power-Assisted Needle Insertion

Device Intervention

Sponsors & Collaborators

  • X9, Inc.

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-04-14
Primary Completion
2026-04-30
Completion
2026-04-30

Countries

  • Uzbekistan

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 NCT07548151 on ClinicalTrials.gov