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Multicenter, observational and prospective study.
Full description
The data collection period will include 6 consecutive months, starting from the date of acceptance or conformity of the CEIC. Or, until an adequate sample size is reached that guarantees the statistical relevance of said analysis. All patients will subsequently be followed up 3 months after discharge from the ICU.
Enrollment
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Inclusion criteria
Exclusion criteria
-under 18 years old
800 participants in 2 patient groups
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Central trial contact
Elena Cuenca Fito
Data sourced from clinicaltrials.gov
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