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Assessment of applicability of an advance directive in the ICU by treating physicians and relatives

Assessment of applicability of an advance directive in the ICU by treating physicians and relatives

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00005360
Enrollment
50
Registered
2013-11-08
Start date
2013-09-12
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

critically ill patients

Interventions

Group 1: Treating ICU-physicians, nurses, other therapists and relatives of included patients are questioned once during the patients ICU stay. Relatives and/or surviving patients are questioned once

Sponsors

Center for Sepsis Control and Care (CSCC)Universitätsklinikum Jena
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Non-competent intensive care patients with AD >18 years

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

MeasureTime frame
Frequency of valid advance directives (AD) according to at least one valid applicability condition by the treating intensive care physician

Secondary

MeasureTime frame
Criteria of validity, discrepant assessment of validity by other caregivers and relatives, discomfort about following written wishes, life-sustaining measures, therapy limitations.

Countries

Germany

Contacts

Public ContactNadja Helke Leder

Universitätsklinikum JenaKlinik für Anästhesie und Intensivmedizin JenaEIDECS

nadja.leder@med.uni-jena.de0177/3518882

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026