Clinical Trials Directory

Trials / Completed

CompletedNCT04877353

Postoperative Noninvasive Ventilation After Upper Abdominal Surgery in Chronic Obstructive Lung Disease

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (actual)
Sponsor
South Valley University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

In Qena university hospital a prospective, randomized study was carried out on 100 COPD patients, all were divided into; conventional therapy without NIV (C group) 50 patients or with prophylactic NIV(N group) 50 patients.NIV applied for approximately 30 to 45 min at 2- to 4-h intervals for 48 h following surgery . Primary endpoint was the acute respiratory events (ARE) .Secondary endpoints were acute respiratory failure (ARF), intubation rate, mortality rate, infectious and non-infectious complications, and ICU stay.

Conditions

Interventions

TypeNameDescription
DEVICENIVNIV applied for approximately 30 to 45 min at 2- to 4-h intervals for 48 h following surgery

Timeline

Start date
2019-01-01
Primary completion
2020-03-30
Completion
2020-11-15
First posted
2021-05-07
Last updated
2021-05-07

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04877353. Inclusion in this directory is not an endorsement.

Postoperative Noninvasive Ventilation After Upper Abdominal Surgery in Chronic Obstructive Lung Disease (NCT04877353) · Clinical Trials Directory