Clinical Trials Directory

Trials / Completed

CompletedNCT05549232

Hypoxic Red Blood Cells for Burns and Hematological Malignancies at Haukeland University Hospital

A Single Center, Pilot Clinical Investigation of Surgical Bleeding in Burn Patients, and Chronically Transfused Patients With Haematologic Malignancies, Who Are Transfused With Hypoxic Red Blood Cells Manufactured With Hemanext ONE System

Status
Completed
Phase
Study type
Observational
Enrollment
22 (actual)
Sponsor
Hemanext · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The overall objective of this study is to collect preliminary safety data on the transfusion of hypoxic RBCs, manufactured with the Hemanext ONE device, in patients with burns and patients with hematological malignancies. The Hemanext ONE device received CE mark in April 2021.

Detailed description

The primary objective is to assess hypoxic RBCs safety and tolerance assessment up to 24 hours following the transfusion initiation and overall up to 7 days (+/- 1 day) after the transfusion episode (single transfusion course). Secondary objectives include the following. 1. Assessment of pre and post transfusion hemoglobin levels 2. Assessment of hemoglobin level before the following transfusion, if applicable 3. Assessment of AEs occurrence: i. Up to 7 days (+/- 1 day) post transfusion, in comparison with historical control (including but not limited to infection, deep vein thrombosis, acute respiratory distress syndrome, transfusion-related acute lung injury, transfusion associated circulatory overload, anaphylactic shock, acute hemolytic transfusion reaction). ii. Up to the subsequent transfusion episode or up to 28 days (+/- 1 day) after the initial transfusion, whichever comes first. iii. From enrollment, up to their subsequent transfusion or 28 days (+/- 1 day) post transfusion, whichever comes first, through the assessment of patient's diary. 4. Assessment of the vital signs during and up to 15 minutes after the transfusion.

Conditions

Interventions

TypeNameDescription
DEVICEHypoxic Red Blood CellsHypoxic Red Blood Cells manufactured with the Hemanext ONE device- CPD/PAGGSM Red Blood Cells, Leukocytes Reduced, and O2/CO2 Reduced

Timeline

Start date
2022-08-24
Primary completion
2024-05-16
Completion
2024-05-16
First posted
2022-09-22
Last updated
2025-07-23
Results posted
2025-05-18

Locations

1 site across 1 country: Norway

Regulatory

Source: ClinicalTrials.gov record NCT05549232. Inclusion in this directory is not an endorsement.