ICU dialysis: which dose of blood thinner works best?
NCT ID NCT07469072
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares two starting doses (20 mg/h vs. 50 mg/h) of the blood thinner nafamostat in ICU patients receiving continuous kidney dialysis. The goal is to see which dose keeps the dialysis filter from clotting longer while avoiding dangerous bleeding. About 92 adults will be randomly assigned to one of the two doses, and doctors will track how long each filter lasts.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Nafamostat Mesilate (a blood-thinning drug)
- What this could lead to
- If it works, this could help doctors choose the best dose of nafamostat to keep dialysis filters working longer and reduce bleeding risks in ICU patients.
- What could go wrong
- This is a small, early-phase trial (92 people) at one hospital, so results may not apply to all patients. The drug can cause bleeding, and the higher dose may not be safer or more effective.
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
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 92 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Jun 2027
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 to 80 years
- 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: 1. Age \& Gender: Aged 18 to 80 years, regardless of gender. 2. Clinical Indication: Admitted to the Intensive Care Unit (ICU) with a confirmed indication for Continuous Renal Replacement Therapy (CRRT) and an expected treatment duration of greater than 24 hours. 3. Coagulation Status: Normal coagulation function prior to CRRT initiation, defined as:International Normalized Ratio (INR) ≤ 1.5,Fibrinogen (FIB) ≥ 1.5 g/L,Activated Partial Thromboplastin Time (APTT) ≤ 45 seconds 4. Platelet Count: Platelet count (PLT) ≥ 50 × 10⁹/L. 5. Body Mass Index (BMI): 18.5 kg/m² ≤ BMI ≤ 25 kg/m². 6. Informed Consent: Written informed consent obtained from the patient or their legally authorized representative. Exclusion Criteria: 1. Hypersensitivity: Known allergy or hypersensitivity to Nafamostat Mesilate or any component of the formulation. 2. Active Bleeding: Presence of active bleeding or a high risk of bleeding that contraindicates anticoagulation (e.g., active gastrointestinal bleeding, intracranial hemorrhage, or recent major surgery with a high bleeding risk). 3. Pregnancy/Lactation: Pregnant or breastfeeding women. 4. Concurrent Anticoagulation: Current use of other systemic anticoagulants (e.g., unfractionated heparin, low molecular weight heparin, warfarin, or direct oral anticoagulants) that cannot be discontinued. 5. Concurrent Extracorporeal Support: Concurrent use of other extracorporeal life support or blood purification therapies that may interfere with coagulation assessment, such as Extracorporeal Membrane Oxygenation (ECMO), Intra-Aortic Balloon Pump (IABP), or Plasma Exchange (PE). 6. Severe Liver Dysfunction: Severe hepatic impairment (Child-Pugh Class C) or baseline total bilirubin levels exceeding 5 times the upper limit of normal. 7. Limited Life Expectancy: Expected survival time of less than 24 hours due to the progression of underlying disease. 8. Conflicting Trials: Current participation in another interventional clinical trial that may influence the outcomes of this study.
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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.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Department of Critical Care Medicine of Zhujiang Hospital,Southern Medical University
RECRUITINGGuangzhou, Guangdong, 510282, China
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