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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02671916
Other study ID # QOL_2015_HIRS
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date January 2015
Est. completion date December 2018

Study information

Verified date March 2019
Source Klinik Hirslanden, Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The goal is to capture the Quality of life and survival of patients one year after the stay at ICU. Data will be collected during the stay in the ICU and evaluated. One year after the ICU stay patients will be send a Quality of Life questionnaire they need to fill out and return. All data will be evaluated together.


Description:

no detailled description necessary


Recruitment information / eligibility

Status Terminated
Enrollment 55
Est. completion date December 2018
Est. primary completion date December 2018
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- patients who are at least 5 days or longer without interruption at the ICU

Exclusion Criteria:

- patients with less than 4 days at the ICU

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
questionnaire
Investigation on all study patients, no Intervention, no groups

Locations

Country Name City State
Switzerland Klinik Hirslanden Zurich Kanton Zurich

Sponsors (1)

Lead Sponsor Collaborator
Prof. Dr. med. Cristoph Haberthür

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survival 1 year after ICU discharge
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