Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06150742

Nafamostat Efficacy in Phase 3 Registrational CRRT Study

Led by Talphera, Inc · Updated on 2025-10-15

70

Participants Needed

10

Research Sites

67 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

A prospective, randomized, placebo-controlled clinical study to investigate the safety and efficacy of Niyad (nafamostat mesylate) for anticoagulation of extracorporeal blood circulating through a dialysis filter in patients undergoing CRRT who cannot tolerate heparin or are at higher risk for bleeding.

CONDITIONS

Official Title

Nafamostat Efficacy in Phase 3 Registrational CRRT Study

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients requiring CRRT or undergoing CRRT initiated within the prior 48 hours
  • Patients who cannot tolerate heparin or are at high risk of bleeding
Not Eligible

You will not qualify if you...

  • Patients weighing less than 50 kg
  • Patients receiving systemic anticoagulation
  • Patients with active bleeding

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 10 locations

1

University of California Los Angeles

Los Angeles, California, United States, 90095

Actively Recruiting

2

AdventHealth

Orlando, Florida, United States, 32804

Not Yet Recruiting

3

Henry Ford Health

Detroit, Michigan, United States, 48202

Actively Recruiting

4

University of New Mexico

Albuquerque, New Mexico, United States, 87131

Actively Recruiting

5

Northwell Health

Great Neck, New York, United States, 11021

Actively Recruiting

6

Mount Sinai

New York, New York, United States, 10029

Actively Recruiting

7

Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio, United States, 45229

Actively Recruiting

8

University of Pittsburgh Medical Center

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

9

Medical University of South Carolina

Charleston, South Carolina, United States, 29425

Actively Recruiting

10

Baylor University Medical Center

Dallas, Texas, United States, 75246

Actively Recruiting

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Research Team

N

Nazneen Patel

CONTACT

C

Chris Houchins

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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