Early Feasibility Study to Assess the Safety and Effectiveness of the OnePoint Dialysis CannulaTM as a Single-Site Vascular Access Device for Hemodialysis Procedures

Starting soon · Not applicable

Conditions studied: Vascular Access

In brief

This is an early feasibility, pre-market, prospective, interventional, single-arm, non-randomized / open-label study intended to support a future pivotal IDE study for eventual FDA clearance of the study device based on the safety and efficacy of the device in cannulating arteriovenous fistulas (AVFs) for hemodialysis procedures.

Key facts

Study ID

NCT07599085

Run by

Evolve Medicus, Inc.

People needed

20

Starts

2026-08-01

Expected to finish

2027-08-01

Last updated by the study team

2026-05-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject is an adult patient ≥ 18 years of age.
• Subject with the ability to attend "in-center" hemodialysis.
• Subject has a requirement of hemodialysis 3 times/week.
• Subject has an AVF that was determined to be mature by standard clinical definition
• Subject with ≥ 3 months stable in center hemodialysis with >90 days use of an AV fistula cannulated with 2 needles with no evidence of stenosis or thrombosis.
• Subject has an AVF that meets all of the following Rule of 5s:
• Flow ≥ 500 mL/min
• Diameter ≥ 5 mm
• Depth ≤ 5 mm from the skin surface
• Length ≥ 5 cm usable for cannulation
• Subject does not have any established lesions or stents in the access circuit as confirmed by ultrasound.
• Subject dialyzes at a center that can confirm 30-day data collection on cannulations and is willing to cooperate in performing real-time assessments and record keeping per Sponsor requirements, to assure subject safety requirements.

You may not qualify if…

• Subject has an existing arteriovenous graft.
• Subject has any active infection within the past 90 days.
• Subject is currently receiving or planning home hemodialysis.
• Subject has a distorted anatomy and/or local vascular injury.
• Subject has a change in blood thinner regimen in the last 60 days.
• Subject has any unstable medical or psychiatric conditions likely to impair their ability to participate in the study.
• Subject has a known history of clinically significant IV drug use.
• Subject is a pregnant or nursing woman, or anticipates pregnancy in the next 3 months.
• Subject is enrolled in another study that could confound the results of this study, without documented pre-approval.
• Subject has a known allergy to plastics.
• Subject is unwilling to sign the study's consent form.
• Subject has a life expectancy of less than 12 months.

Full record on ClinicalTrials.gov

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