Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 6:55 PM
Ignite Modification Date:
2025-12-24 @ 6:55 PM
NCT ID:
NCT02679157
Eligibility Criteria:
Inclusion Criteria:
ICU stay\>24 hours for postoperative patients and \>12 hours for other ICU admissions
Exclusion Criteria:
1. Previously documented cognitive impairment (e.g. dementia or intellectual development disorder resulting in poor understanding/compliance in outcome assessment)
2. No home address
3. Unable to read and write in language spoken at local study site (Swedish/Danish/Dutch)/used in questionnaires
4. Patient declines participation
5. Moribund patient or with more than one limitation of therapy
6. Need for neurointensive care due to head trauma, intracranial hemorrhage or infarction AND GCS never better than 13 in the first 48 hours
7. Transfer to other ICU before discharge to ward
8. Solely in ICU for elective procedure (eg central line, epidural)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02679157
Study Brief:
Protocol Section:
NCT02679157