Insufficient cellular oxygen in ICU patients with anaemia: the INOX ICU-2 Study
- Conditions
- anemie bij kritisch zieke mensen op de ICanaemiaanemia
- Registration Number
- NL-OMON50343
- Lead Sponsor
- eids Universitair Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 209
During the pilot study: all adult patients, admitted to the intensive care unit
with [Hb] below 6,3 mmol/l, who are planned to undergo a transfusion of red
blood cells.
During the prospective cohort study: all patients with a Hb below 6.3 mmol/l in
whom an arterial catheter is in place and in whom a red cell transfusion is
planned.
-adults without an legal representative for the informed consent,
-less than 18 years old,
-patients in need of emergency red cell transfusion e.g. bleeding,
-porphyria,
-known photodermatosis,
-ICU stay <24hrs,
-pregnant or breast feeding women since there is no adequate data from the use
of ALA in pregnant or breast feeding women,
-hypersensitivity to the active substance or to the plaster material of ALA,
-insufficient comprehensibility of the Dutch language
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method