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NOT YET RECRUITING
NCT07643597

Volume Removal Intolerance During Net Ultrafiltration in Acute Kidney Injury Patients

Sponsor: Hospital Las Higueras

View on ClinicalTrials.gov

Summary

Acute kidney injury (AKI) is common in critically ill patients and is frequently associated with fluid overload, which can worsen clinical outcomes. Continuous renal replacement therapy (CRRT) allows fluid removal through net ultrafiltration (UFNET), but some patients develop hemodynamic instability or signs of poor tissue perfusion during this process. The purpose of this prospective observational study is to evaluate tolerance to net ultrafiltration in critically ill patients with AKI receiving CRRT. The study will assess clinical, hemodynamic, ultrasound, perfusion, and biochemical parameters before and during fluid removal to identify factors associated with ultrafiltration intolerance. The investigators hypothesize that alterations in hemodynamic, perfusion, and congestion-related parameters can identify patients at increased risk of ultrafiltration intolerance before the development of overt hypotension. The results may help improve individualized fluid removal strategies and optimize the safety of CRRT in critically ill patients.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

128

Start Date

2026-07-06

Completion Date

2027-12-01

Last Updated

2026-06-11

Healthy Volunteers

No

Locations (10)

Hospital Cárdio Pulmonar

Salvador, Brazil

Hospital Clínico Regional de Concepción

Concepción, Chile

Complejo Asistencial Dr. Victor Ríos Ruiz

Los Ángeles, Chile

Hospital Clínico Dra. Eloísa Díaz Insunza de La Florida

Santiago, Chile

Hospital Las Higueras de Talcahuano

Talcahuano, Chile

Hospital Universitario San José de Popayán

Popayán, Colombia

Hospital General Enrique Garces

Quito, Ecuador

Ospedale San Bortolo

Vicenza, Italy

Hospital General de Mexico

Mexico City, Mexico

Hospital Nacional Cayetano Heredia

Lima, Peru