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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03184623
Other study ID # nWMO 205
Secondary ID
Status Completed
Phase N/A
First received June 9, 2017
Last updated September 5, 2017
Start date June 9, 2017
Est. completion date September 5, 2017

Study information

Verified date September 2017
Source Medical Centre Leeuwarden
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

ICUacquired weakness is a common complication of critical illness, particularly in patients receiving mechanical ventilation and/or suffering from conditions leading to the systemic inflammatory response syndrome.


Description:

The weakness and disability that result from these neuromuscular disorders can dominate the lont-term course and impede recovery.

In this observational study we try to measure muscle mass and body composition by echocardiography and BIVA at admission and on day 2, 5


Recruitment information / eligibility

Status Completed
Enrollment 23
Est. completion date September 5, 2017
Est. primary completion date September 5, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- all acute admitted patients in ICU

Exclusion Criteria:

- age < 18

- stay on ICU < 48 hours

- use of corticosteroids

- neurological diseases

- acute kidney injure / nead of CVVH

Study Design


Related Conditions & MeSH terms


Intervention

Other:
muscle mass measurement
measurement of muscle mass by echocardiography

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 change in muscle mass measurements during ICU stay measurement by echography baseline, day 2 and day 5
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