NCT05418816Active, not recruiting
SelfWrap-Assisted Arteriovenous Fistulas
Initial Feasibility Study of SelfWrap-Assisted Arteriovenous Fistulas (SW-AVF)
Source: ClinicalTrials.gov · Last updated 1 Apr 2025
Brief summary (registry, in English)
This is a single-center, prospective, single-arm clinical study to evaluate the feasibility, safety, and performance of VenoStent's SelfWrap® Bioabsorbable Perivascular Wrap on arteriovenous fistulas (AVFs). All participants are chronic kidney disease (CKD) patients already receiving hemodialysis treatments that are referred for creation of a new arteriovenous fistula (AVF).
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 20 (actual)
- First submitted
- 7 Jun 2022
- Start date
- 14 Jun 2021
- Primary completion date
- 23 Feb 2022
- Lead sponsor
- VenoStent
- Diseases
- Chronic kidney disease
- NCT number
- NCT05418816
What you commit to
- Study type: Interventional
- Participants enrolled: 20
- From 14 Jun 2021 to the primary completion date, 23 Feb 2022
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Twelve months or longer with a catheter, on the planned side of AVF creation; or if there has been any previously failed AVF and AVG on the planned side of AVF creation.
- Significant (\> 50%) stenosis at the target vein on the side of surgery, as diagnosed by preoperative ultrasound;
- Prior steal on the side of surgery;
- Enrolled in another investigational drug, device, or biological study and has not completed the primary endpoint(s), or was previously enrolled in this study;
- Patient expecting to undergo kidney transplant surgery within 12 months of enrollment;
Other illness
- Planned index procedure to revise or repair an existing fistula;
- Abnormal cardiac rhythm;
- Known coagulation disorder;
- Known or suspected active infection at the time of surgery;
- Congestive heart failure NYHA class 4;
- Patient has a comorbid condition that, in the judgment of the Investigator, may cause him/her to be non-compliant with the protocol or confound data interpretation.
Other
- Known central venous stenosis \> 50%;
- Amputated limb;
- Use of a peripherally-inserted central catheter (PICC) line;
- Life expectancy less than 12 months;
- Unwillingness or inability to give consent and/or comply with the study follow up schedule.
Who the study is looking for
- Age ≥ 18 years, male or female;
- Subjects already receiving hemodialysis treatments that are ultimately referred for a new AVF, per current US KDOQI Clinical Practice Guidelines for Vascular Access updated in 2019 which recommend an AVF or arteriovenous graft (AVG) consistent with patient life-plan, overall goals of care, and anticipated duration of hemodialysis; if life expectancy \> 1 year, recommend forearm AVF, forearm AVG, or upper arm AVF; if \< 1 year, recommend forearm AVG/upper arm AVG; if urgent start, early cannulation AVG or central venous catheter (CVC);
- Target cephalic vein inner diameter ≥ 2.5 mm and target artery ≥ 2.0 mm as measured via duplex ultrasound with a tourniquet applied;
- For radial AVFs, a nonpathological modified Allen test;
- Triphasic arterial flow and intact venous outflow;
- A vascular access site being used for hemodialysis that is either positioned contralateral to the planned AVF creation surgery or located in the groin. If the catheter is positioned on the same side as the planned AVF, the catheter will be moved to the other arm prior to the AVF created surgery.
- Participant is willing and able to comply with study requirements and sign an informed consent.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Sanatorio Italiano Coordinator of this site? Confirm its status | Asunción | Paraguay | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.