endoAVF vs surgAVF for Chronic Kidney Failure
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores two methods to create an arteriovenous fistula (AVF), a vital connection between an artery and a vein for patients with end-stage kidney disease requiring hemodialysis. Traditionally, surgeons create AVFs, but a less invasive method now uses endovascular techniques, avoiding general anesthesia and involving a device that passes through the skin. The trial compares outcomes of the traditional surgical method (surgAVF) with the newer method (endoAVF, or Endovascular Arteriovenous Fistula) to determine which is more effective or preferable for patients. Individuals who have chosen hemodialysis and have suitable arm vein sizes may qualify to participate. As an unphased trial, this study allows patients to contribute to medical advancements and potentially benefit from innovative treatment options.
Do I need to stop my current medications for this trial?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
What prior data suggests that these devices are safe for creating arteriovenous fistulas?
Research shows that creating an endovascular arteriovenous fistula (endoAVF) is generally well-tolerated by patients. A review of studies found that endoAVF procedures are safe and have few side effects. Patients undergoing this treatment often experience fewer complications compared to traditional surgery. Additionally, endoAVF does not require general anesthesia, reducing anesthesia-related risks.
The FDA has approved devices used for endoAVF, such as the WavelinQ™ and Ellipsys® systems, indicating they meet safety standards. While researchers continue to collect long-term safety data, early results are encouraging.
In contrast, surgAVF involves surgery with general anesthesia, which can lead to more risks, such as infections or anesthesia-related issues. However, both methods create arteriovenous fistulas, essential for patients on dialysis.
Overall, both treatments are considered safe, but endoAVF is less invasive.12345Why are researchers excited about this trial?
Researchers are excited about endoAVF and surgAVF because they offer innovative ways to create arteriovenous fistulas for patients with chronic kidney failure. EndoAVF is particularly unique due to its minimally invasive approach, using devices like the WavelinQ™ EndoAVF System and the Ellipsys® Vascular Access System. This method avoids the need for general anesthesia and large incisions, unlike traditional surgical methods. On the other hand, surgAVF requires a more invasive surgical procedure with general anesthesia, which is the current standard of care. Both treatments aim to improve patient outcomes and comfort, making them promising options for those requiring dialysis access.
What evidence suggests that this trial's treatments could be effective for chronic kidney failure?
This trial will compare the effectiveness of endoAVF (endovascular arteriovenous fistula) with surgAVF (surgical arteriovenous fistula) for patients needing hemodialysis. Research has shown that creating an endoAVF is promising, as it avoids major surgery by using devices to connect blood vessels through the skin and requires only local anesthesia. Studies have found that endoAVFs are successful and remain open over time, similar to traditional surgical AVFs. They are also considered safe, with fewer surgery-related complications. These findings suggest that endoAVF could effectively serve as an alternative to surgAVF for creating the access needed for dialysis.12456
Who Is on the Research Team?
Karen Woo, MD, PhD
Principal Investigator
University of California, Los Angeles
Are You a Good Fit for This Trial?
This trial is for adults over 18 with end-stage kidney disease who need hemodialysis and have veins in their arms suitable for creating a vascular access. They must be able to consent to the study, not pregnant, nor planning pregnancy within six months, and not opting for peritoneal dialysis or a kidney transplant soon.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Pre-operative Evaluation
Vein mapping and duplex ultrasound imaging to determine anatomical suitability for AVF creation
Treatment
Participants undergo either endoAVF or surgAVF procedure based on randomization
Follow-up
Participants are monitored for safety and effectiveness after treatment, with routine follow-ups and monthly chart reviews
Registry Follow-up (optional)
Participants who opt for the registry have their clinical outcomes tracked via medical record data abstraction
What Are the Treatments Tested in This Trial?
Interventions
- endoAVF
- surgAVF
endoAVF is already approved in United States for the following indications:
- Creation of arteriovenous fistula for hemodialysis access
- Creation of arteriovenous fistula for hemodialysis access
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of California, Los Angeles
Lead Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Collaborator