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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03169452
Other study ID # NIV
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 1, 2017
Est. completion date November 2018

Study information

Verified date June 2018
Source Assiut University
Contact Sahar Mohamed, MBBCh
Phone 00201069916415
Email saharmuhammad25@yahoo.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Noninvasive ventilation is increasingly used method of respiratory management in both the emergency room and critical care. Noninvasive ventilation delivers mechanically assisted breaths without the placement of an artificial airway and has become an important mechanism of ventilator support inside and outside the intensive care unit.

Noninvasive ventilation is further subdivided into negative pressure ventilation which is the iron lung, first used in 1928 and the Hayek oscillator, is a more recently designed to provide negative pressure during inspiration and positive pressure during expiration. Noninvasive positive pressure ventilation can be used as continuous positive airway pressure or bi-level positive airway pressure.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date November 2018
Est. primary completion date August 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- obstructive sleep apnea syndrome

- acute exacerbation Chronic obstructive pulmonary disease

- pneumonia

- interstitial lung diseases

Exclusion Criteria:

- Patients refuse Non invasive ventilation

- Patients with absolute indication for Mechanical ventilator (in respiratory arrest or unstable cardiorespiratory status, trauma or burns involving the face, or gastric surgery, reduced consciousness, Pneumothorax

- Patients with contraindication to Non invasive ventilation

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Non-invasive mechanical ventilator
mechanical assisted breaths without the placement of an artificial way

Locations

Country Name City State
Egypt Assiut University Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary percentage of patients need mechanical ventilation the number of patients without improvement on non-invasive ventilator and require transfer to mechanical ventilator 1-48 hours
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