Could permanent dialysis access replace catheters in ICU kidney therapy?
NCT ID NCT07447128
First seen Jun 25, 2026 · Last updated Jul 07, 2026 · Updated 3 times
Summary
This study looks at whether using a patient's permanent dialysis access (a fistula or graft) instead of a temporary catheter is safe and effective for delivering continuous kidney replacement therapy in the ICU. Researchers will enroll 50 adults with end-stage kidney disease who are in the ICU and need this therapy. The goal is to develop a standard procedure and see if the access stays usable without complications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Cannulation of permanent dialysis access (arteriovenous fistula or graft) for continuous renal replacement therapy
- What this could lead to
- If successful, this could lead to a safer, standard way to deliver continuous kidney therapy in the ICU, reducing infections and blood vessel damage from repeated catheter use.
- What could go wrong
- This is a small, early feasibility study with only 50 participants, so results may not apply broadly. The procedure requires highly trained staff and may not be practical in all ICU settings.
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
-
About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Jul 2026
An estimate. Start dates often move.
- Expected to finish
-
Dec 2027
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: 1. Age ≥18 years. 2. ESKD patients on chronic hemodialysis for \>1 year in duration who are admitted to the ICU and in need of CRRT. 3. Anticipated CRRT duration ≥24 hours, based on clinical assessment of the renal trajectory. 4. Patient with functioning arteriovenous access, either arteriovenous fistula or arteriovenous graft. 5. Expected mechanical ventilation for a minimum of 12 hours, based on clinical assessment of the underlying diagnosis. 6. Expected Richmond Agitation Sedation Scale (RASS) goal of 0 or less for a minimum of 12 hours, based on clinical assessment of the underlying diagnosis. 7. Patients able to tolerate placement of an arm board at the vascular access site. 8. Baseline AVA blood flow of at least 600 mL/min for AVG and 500 mL/min for AVF during ultrasonography evaluation upon enrollment. Exclusion Criteria: 1. Age less than 18 years old. 2. Patients who receive dialysis via hemodialysis catheter or existing central catheter suitable for hemodialysis. 3. ESKD patients who, at the time of enrollment, have a sacral pressure ulcer or other clinically significant skin integrity impairment requiring frequent repositioning, extensive patient rotation, or advanced wound care management. 4. Patients with elevated INR above 5 at the time of study enrollment. 5. Patients with acute liver failure, defined as AST \>1000 U/L and/or ALT \>1000 U/L at the time of study enrollment. 6. Patients with a platelet count of less than 50,000 (10⁹ plt/L) at the time of study enrollment. 7. Patients with evidence of disseminated intravascular coagulation at the time of study enrollment. 8. Known pregnancy at the time of study enrollment. 9. Patients at high risk for rapid clinical deterioration, or those deemed unsuitable for AVA-based CRRT by the prescribing nephrologist or ICU physician.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Continuous renal replacement therapy (CRRT) are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
East Carolina University Medical Center
Greenville, North Carolina, 27834, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a blood thinner cut stroke risk in dialysis patients?
- Fluid overload hides true lung pressure in dialysis patients, study aims to unmask it
- Diabetes drug semaglutide tested in dialysis patients for safety
- Can extra protein save muscle in dialysis patients?
- New graft could make dialysis easier for kidney patients
- New blood thinner may improve dialysis outcomes in sepsis patients