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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02920281
Other study ID # WEAN SLEEP 1
Secondary ID
Status Completed
Phase N/A
First received September 29, 2016
Last updated January 12, 2018
Start date November 2014
Est. completion date April 2017

Study information

Verified date January 2018
Source Poitiers University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to evaluate the impact of sleep quality on the length of mechanical ventilation weaning, in intensive care unit patients


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date April 2017
Est. primary completion date April 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Mechanical ventilation for at least 24 hours before the first weaning test

- difficult weaning of mechanical ventilation defined as failure to the first weaning test

- patients aged at least of 18 years

Exclusion Criteria:

- peripheral or central nervous system pathology

- known psychiatric pathology or agitation

- clinical worsening before polysomnography (shock with vasopressor drugs, coma with Glasgow scale < 8, PaO2/FiO2 ratio < 150 with respiratory distress signs)

- pregnant or breastfeeding women

- patient under legal guardianship or protection

- patient with no health insurance coverage

- age < 18 years

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Polysomnography


Locations

Country Name City State
France CHU Poitiers Poitiers

Sponsors (1)

Lead Sponsor Collaborator
Poitiers University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Compare the length of weaning patients who have a poor quality of sleep to those who have a good quality sleep. 24 hours
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