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Post Market Study for VasQ, an External Support Implant for Arteriovenous Fistula
NCT06516653 · View on ClinicalTrials.gov ↗
Study Summary
VasQ is an external support implant for arteriovenous fistulas created for dialysis access. This is a postmarket surveillance, prospective, multi-center, randomized, controlled, open label trial enrolling 300 patients randomized into two study arms: * Treatment arm: End to side fistula supported with VasQ * Control: Standard of care end to side fistula
Conditions Studied
Interventions
- DEVICE VasQ
- PROCEDURE Arteriovenous fistula creation for dialysis vascular access
Study Locations (7)
California
- Fresenius Vascular Care Long Beach — Long Beach
Florida
- Sarasota Memorial Hospital — Sarasota
Massachusetts
- Brigham and Women's Hospital — Boston
Mississippi
- Greenwood Leflore Hospital — Greenwood
Nevada
- Azura Surgery Center Las Vegas — Las Vegas
South Carolina
- Fresenius Vascular Care Columbia — Columbia
Virginia
- Fairlawn Surgery Center — Roanoke
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 300 participants |
| Start Date | 2025-01-13 |
| Est. Completion | 2028-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06516653
The ClinicalTrials.gov registry entry for NCT06516653 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Laminate Medical Technologies, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with End Stage Renal Disease appearing as the primary indexed condition, and to 2 interventions — of which VasQ is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06516653 reports 7 study locations spanning 7 distinct geographic areas — top geographies include California, Florida, Massachusetts. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06516653 about?
NCT06516653 is a clinical study titled "Post Market Study for VasQ, an External Support Implant for Arteriovenous Fistula". VasQ is an external support implant for arteriovenous fistulas created for dialysis access. This is a postmarket surveillance, prospective, multi-center, randomized, controlled, open label trial enrolling 300 patients randomized into two study arms: * Treatment arm: End to side fistula supported w...
What is the current status of trial NCT06516653?
This trial is currently recruiting. It is a NA study. The enrollment target is 300 participants. The study started on 2025-01-13. Estimated completion is 2028-05.
What conditions does trial NCT06516653 study?
This clinical trial studies the following conditions: End Stage Renal Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06516653?
The interventions under investigation include: VasQ (DEVICE), Arteriovenous fistula creation for dialysis vascular access (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06516653?
This trial is sponsored by Laminate Medical Technologies, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06516653 being conducted?
This trial has 7 study locations across California, Florida, Massachusetts, Mississippi, Nevada. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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