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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01817608
Other study ID # 107589
Secondary ID
Status Completed
Phase N/A
First received March 15, 2013
Last updated March 20, 2013
Start date September 2004
Est. completion date June 2011

Study information

Verified date March 2013
Source Loyola University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The investigators objective is to assess quality of life and functional outcome in patients requiring short-term mechanical ventilation. Additionally, the investigators plan to measure the recovery of peripheral muscle strength and respiratory muscle strength during recovery.


Recruitment information / eligibility

Status Completed
Enrollment 66
Est. completion date June 2011
Est. primary completion date June 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- ICU patients who require mechanical ventilation for at least 2 days

- the ability to speak English

- willing to participate

Exclusion Criteria:

- patients who require mechanical ventilation at home before hospitalization

- patients previously requiring mechanical ventilation at an LTAC facility

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Loyola University Chicago Health Sciences Division Maywood Illinois

Sponsors (1)

Lead Sponsor Collaborator
Amal Jubran

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary quality of life scores SF-36, Katz, respiratory muscle strength and handgrip strength will be measured up to one year after discharge No
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