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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02706457
Other study ID # nWMO 143
Secondary ID
Status Completed
Phase N/A
First received February 16, 2016
Last updated April 11, 2016
Start date October 2015
Est. completion date April 2016

Study information

Verified date April 2016
Source Medical Centre Leeuwarden
Contact n/a
Is FDA regulated No
Health authority Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
Study type Observational

Clinical Trial Summary

Barthel Index and demographic variables of patients were collected to investigate the question whether the improvements of the functionality improves the Barthel Index over the years.


Description:

idem


Recruitment information / eligibility

Status Completed
Enrollment 849
Est. completion date April 2016
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years and older

- length of stay longer than 48 hours

Exclusion Criteria:

- no exclusion criteria if inclusion is correct

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Other:
Barthel index for functionality
The Barthel Index for functionality is done standard in all patients after intensive care admission

Locations

Country Name City State
Netherlands Medical Center Leeuwarden Leeuwarden

Sponsors (1)

Lead Sponsor Collaborator
Medical Centre Leeuwarden

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Difference in Barthel Index barthel index is analyzed over the years 2012 - 2014 from januari 2012 until decembre 2014 No
Secondary Relation between Barthel Index and length of stay in ICU from januari 2012 until decembre 2014 No
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