Swecrit Biobank - Blood Samples From Critically Ill Patients and Healthy Controls
Condition(s) studied
Investigational drug(s) / intervention(s)
Blood collection: Sampling on admission to ICU (all patients)
Blood collection, serial sampling: Additional sampling to admission samples in 1. the Cardiac Arrest group after 12 and 48 hours 2. the Covid-19 group on day 2 and 7 while in the ICU 3. the Covid-19 group after 3 and 12 months.
Study summary
Blood samples are collected and stored in a biobank for later analysis of circulating substances in peripheral blood and genetic variations in patients with severe critical illness and risk of death. The aim is to analyze stored samples in order to identify substances that can help predict the outcome of critically ill patients, but also to optimize treatment and possibly prevent serious illness and death in the future.
Eligibility
Primary outcome measure(s)
- Mortality (all) — 6 months
Primary outcome when functional outcome cannot be assessed.
Trial sites (4)
| Facility | City | Region | Status |
|---|---|---|---|
| Helsingborg Hospital | Helsingborg | Sweden | |
| Kristianstad Central Hospital | Kristianstad | Sweden | |
| Skane University Hospital | Lund | Sweden | |
| Skane University Hospital | Malmö | Sweden |
More Skane University Hospital trials in Sweden
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04974775 on ClinicalTrials.gov ↗ ← All trials in Sweden