New wrist surgery could make dialysis easier for kidney patients
NCT ID NCT02728817
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new surgical method called RADAR for creating blood vessel connections needed for dialysis in 200 people with end-stage kidney disease. The goal is to see if this technique leads to fewer blockages and better long-term function compared to the standard approach. Participants are randomly assigned to receive either the RADAR or traditional fistula surgery, and their outcomes are tracked over time.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- surgical procedure (RADAR technique vs. traditional fistula creation)
- What this could lead to
- If successful, this technique could improve fistula maturation and reduce complications, making dialysis access more reliable for kidney patients.
- What could go wrong
- This is a relatively small, early-stage trial comparing surgical methods, so results may not apply to all patients. The new technique also carries standard surgical risks like infection or bleeding.
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.
- Participants
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200 people
The number who actually took part.
- Started
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Apr 2017
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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: * Patient referred by the nephrologist for the creation of a primary vascular access * Clinical examination of both upper limbs showing on the same limb: * A cephalic vein at the distal third of the forearm * Radial pulse * Ulnar pulse * Positive Allen test (patent palmar arches) * Preoperative arterial and venous duplex ultrasound examination of both limbs showing on the same limb : * A patent cephalic vein, ≥2mm in diameter at the distal 1/3 of the forearm, free from stenosis, ≥15cm in length * A patent on dominant radial artery, ≥2mm in diameter at the distal 1/3 of the forearm, free from stenosis and major calcifications * A patent ulnar artery, free from stenosis and major calcifications * A positive Allen's test with assessment of the retrograde flow (patent palmar aches) * Digital pressure \>50mmHg when occlusive compression is made on the radial artery and digital/brachial ratio \>0.5 Exclusion Criteria: * patient under guardianship
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Aphm
Marseille, France
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CHU de Nice - Service de chirurgie vasculaire
Nice, France
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Polyclinique Les Fleurs
Ollioules, France
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Polyclinique Notre Dame
Draguignan, France
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