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Recruiting NCT05874674

The Safety of Nafamostat Mesylate for Patients With High Risk Bleeding Undergoing Hemodialysis: A Pilot Study

No phase Interventional Dialysis; Complications Bleeding

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Nafamostat Mesylate.
Who it may be relevant to
Registry conditions: Dialysis; Complications, Bleeding. Basic parameters: 18 years — 99 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
South Korea
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Safety of Nafamostat Mesylate for Patients With High Risk Bleeding Diathesis Undergoing Hemodialysis: A Pilot Study

Overview

Comparison nafamostat and low molecular weight heparin among dialysis patients

Interventions

  • Drug Nafamostat Mesylate
    Comparison effect of nafamostat and cnoxan

Primary outcome measures

  • Number of patients with severe bleeding [Time frame: 6 month]
Secondary outcome measures (1)
  • Number of patients with dialysis circuit clot [Time frame: 6 month]

Eligibility criteria

Inclusion criteria

  • platelet below 10k PTT above 60 second INR above 20 patient with bleeding (epistaxis, orbital bleeding, hematuria) recent brain hemorrhage (within 6 months) receiving anticoagulant therapy (coumadin or NOAC) dual antiplatelet agent users received major surgery within one month

Exclusion criteria

  • cancer liver cirrhosis pregnancy drug allergy current bleeding on major organ (brain, gastrointestinal)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Prevention

Study locations

South Korea · 1 center
  • Yonsei Unviersity Wonju College of Medicin — Wŏnju

Publications

  • Natale P, Palmer SC, Ruospo M, Longmuir H, Dodds B, Prasad R, Batt TJ, Jose MD, Strippoli GF. Anticoagulation for people receiving long-term haemodialysis. Cochrane Database Syst Rev. 2024 Jan 8;1(1):CD011858. doi: 10.1002/14651858.CD011858.pub2. PMID 38189593

Identifiers

NCT: NCT05874674 · CR122018

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗