Dialysis fistula fix? study pulled before it began
NCT ID NCT03365089
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aimed to see if tying off extra veins (collaterals) could help dialysis fistulas mature so they can be used for treatment. It planned to enroll patients whose fistulas were not developing properly. However, the trial was withdrawn before any participants were enrolled, so no conclusions can be drawn.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- collateral vein ligation (a procedure to tie off extra veins near the fistula)
- What this could lead to
- If it had worked, this could have pointed to a simple way to help more dialysis fistulas become usable, reducing the need for additional procedures.
- What could go wrong
- The trial was withdrawn before any patients were enrolled, so we have no data on whether the procedure is effective or safe. It remains an unproven idea.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Started
-
May 2018
- Expected to finish
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Mar 2020
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: \- Patients with upper extremity autogenous AVF presenting with FTM with evidence of collaterals on ultrasound and/or clinical exam. Exclusion criteria: * Age under 18 years * Pregnant women * Prior endovascular or surgical procedure in the fistula after its creation (with the exception of surgical superficialization or mobilization) * Clinical evidence of infection associated with the AVF * Uncorrectable coagulopathy (International Normalized Radio \>2.5, platelet count \<50.000/μL) * Absence of significant venous side branches on angiogram (defined as those that arise in the initial 10 cm, including the future cannulation zone, and have maximal diameter greater than or equal to one third of the widest diameter of the fistula's main venous channel in this segment).
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Massachusetts General Hospital
Boston, Massachusetts, 02114, United States
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