Fort Wayne, INNCT06001827Now EnrollingIRB Ready

Chronic Kidney Diseases Clinical Trial in Fort Wayne, IN

Access cutting-edge chronic kidney diseases treatment through this clinical trial at a research site in Fort Wayne. Study-provided care at no cost to qualified participants.

Sponsored by VenoStent

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Expert Care in Fort Wayne

Access chronic kidney diseases specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related chronic kidney diseases treatment provided free

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Check if you qualify for this chronic kidney diseases clinical trial in Fort Wayne, IN

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Fort Wayne

    Convenient for IN residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Fort Wayne site if eligible
  4. 4Begin participation

About This Chronic Kidney Diseases Study in Fort Wayne

This is a prospective, randomized, multi-center clinical trial for chronic kidney disease (CKD) patients referred for creation of a new arteriovenous fistula (AVF) in order to assess the safety and effectiveness of SelfWrap, a bioabsorbable perivascular wrap.

Sponsor: VenoStent

Who Can Participate

Inclusion Criteria

Age of at least 18 years
Referred for creation of a new AVF
Willing and able to comply with study requirements, communicate with the study team, and attend follow up visits over a period of 36 months

Exclusion Criteria

Planned index procedure to revise or repair an existing fistula
Target artery inner diameter \< 2.0 mm, as measured by ultrasound while the target arm is under tourniquet pressure and anesthesia
Target vein inner diameter \< 2.0 mm, as measured by ultrasound while the target arm is under tourniquet pressure and anesthesia
Significant (at least 50%) stenosis at the target vein on the side of surgery (between the planned anastomosis site and the axillary vein), as diagnosed by preoperative ultrasound
Known central venous stenosis of at least 50% on the side of surgery
Presence of a stent or a stent graft within the access circuit
Known or suspected coagulation disorder that, in the opinion of the Investigator, puts too much risk on the patient for AVF creation
Known or suspected active infection at the time of surgery
Congestive heart failure NYHA class 4
Prior steal on the side of surgery;
Enrolled in another investigational drug, device, or biological study, or was previously enrolled in this study
Life expectancy less than 12 months
Expected to undergo kidney transplant surgery within 6 months of enrollment
Expected to undergo home hemodialysis
Females of childbearing potential (premenopausal and not surgically sterile) without documented current negative pregnancy test at screening
Presence of a comorbid condition that, in the opinion of the Investigator, may significantly confound the collection of safety and efficacy data in this study
Unwillingness or inability to give consent and/or comply with the study follow up schedule
Any health condition, which in the opinion of the Investigator, would interfere with the safety of the participant or the participant's ability to comply with the study.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Fort Wayne?

Yes, this clinical trial (NCT06001827) has an active research site in Fort Wayne, IN that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Chronic Kidney Diseases Treatment Options in Fort Wayne, IN

If you're searching for chronic kidney diseases treatment options in Fort Wayne, IN, this clinical trial (NCT06001827) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Fort Wayne research site is actively enrolling participants for this clinical trial. You'll receive care from experienced chronic kidney diseases specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all chronic kidney diseases clinical trials near you to find additional studies recruiting in your area.

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