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Comparison of the Human Acellular Vessel (HAV) With Fistulas as Conduits for Hemodialysis

Completed · Phase 3 · NCT03183245

Conditions: Renal Failure, End Stage Renal Disease, Hemodialysis, Vascular Access

At a glance

Research payments reported, 2025
$211,814
U.S. investigators named
22
Sites paid
22
Planned or actual enrollment
242

About the trial

Sponsor
Humacyte, Inc. (with CTI Clinical Trial and Consulting Services, California Institute for Regenerative Medicine (CIRM))
Tested
Human Acellular Vessel (HAV) (biological), Arteriovenous fistula (AVF) (procedure), Hemodialysis (other)
Dates
Started 2017-09-29; completion 2025-06-19
Results posted
Not yet

The main purpose of this study is to compare the Human Acellular Vessel (HAV) with arteriovenous fistula (AVF) when used for hemodialysis access

From ClinicalTrials.gov, last updated 2025-11-20. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Humacyte Global, Inc. reported $211,814 in research payments for this study in 2025 (42 payments).

Products named: Symvess

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.