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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01526642
Other study ID # 2010/080/HP
Secondary ID
Status Terminated
Phase N/A
First received January 23, 2012
Last updated August 21, 2017
Start date December 2011
Est. completion date December 2015

Study information

Verified date August 2017
Source University Hospital, Rouen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Chronic Obstructive Pulmonary disease (COPD) patients with chronic hypercapnic respiratory failure are more likely to develop exacerbations. Non-invasive ventilation has been proposed to treat acute respiratory failure but little information is available about the benefits of home non-invasive ventilation in COPD patients with chronic hypercapnic respiratory failure surviving an acute hypercapnic respiratory failure. The purpose of this study is to determine whether home non-invasive ventilation can reduce recurrent acute hypercapnic respiratory failure in COPD patients who survived an episode of acute hypoxemic respiratory failure (AHRF) treated by Non-invasive ventilation (NIV).


Recruitment information / eligibility

Status Terminated
Enrollment 12
Est. completion date December 2015
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Age > 18 years old

- COPD patients who survived after an episode of acute hypercapnic respiratory failure

- Patients weaned from ventilation (non invasive ventilation or mechanical ventilation) for acute episode since at least seven days with stable arterial blood gas since at least two days: PaCO2 > 55 mmHg and pH > 7.35

Exclusion Criteria:

- Age > 85 years old

- Non- COPD causes of respiratory failure

- Obstructive sleep apnea excluded by polysomnography

- Adverse psychosocial status

- Serious co-morbidity

Study Design


Intervention

Device:
Non Invasive Ventilation
NIV during night

Locations

Country Name City State
France CHU de Rouen Rouen

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Rouen

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Acute hypercapnic respiratory failure episode up to 102 weeks
Secondary Death 1 month and every 6 months during 2 years
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