Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05148026

Regional Citrate Anticoagulation for RRT During V-V ECMO

Regional Citrate Anticoagulation for Continuous Renal Replacement Therapy During Veno-venous ECMO: a Crossover Randomized Controlled Study

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
University of Milano Bicocca · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Anticoagulation is an essential component of all extracorporeal therapies. Currently locoregional citrate anticoagulation is the recommended technique for continuous renal replacement therapy (CRRT). However, low clearance of citrate restricts its use to blood flow up to 150 mL/min, preventing its use in ECMO. Renal replacement therapy (RRT) is commonly provided to ECMO patients with AKI. In presence of systemic heparinization for ECMO, additional anticoagulation for the CRRT circuit (i.e. RCA) is usually not employed. Nevertheless, thrombosis occurs more frequently in the CRRT circuit than the oxygenator because of the slower blood flow. The aim of this prospective, cross-over study is to assess, in patients undergoing CRRT during veno-venous ECMO (vv-ECMO), the efficacy and safety of adding regional citrate anticoagulation (RCA) for CRRT circuit anticoagulation.

Conditions

Interventions

TypeNameDescription
DRUGUnfractionated heparin + RCA firstPatients are randomized to receive this sequence of anticoagulation regimens: UFH+RCA / UFH / UFH+RCA / UFH / UFH+RCA / UFH
DRUGUnfractionated heparin firstPatients are randomized to receive this sequence of anticoagulation regimens: UFH / UFH+RCA / UFH / UFH+RCA / UFH / UFH+RCA

Timeline

Start date
2021-11-14
Primary completion
2025-10-31
Completion
2026-01-31
First posted
2021-12-08
Last updated
2024-05-08

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT05148026. Inclusion in this directory is not an endorsement.