Postoperative Noninvasive Ventilation After Upper Abdominal Surgery in Chronic Obstructive Lung Disease
Not Applicable
Completed
- Conditions
- Acute Respiratory Failure Post Surgical (Diagnosis)
- Interventions
- Device: NIV
- Registration Number
- NCT04877353
- Lead Sponsor
- South Valley University
- Brief 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Group N NIV 50 patients.NIV applied for approximately 30 to 45 min at 2- to 4-h intervals for 48 h following surgery
- Primary Outcome Measures
Name Time Method acute respiratory events 28days patients %
- Secondary Outcome Measures
Name Time Method acute respiratory failure 28 days patients %
intubation rate 28 days patients %
ICU mortality 28 days patients %
ICU length of stay 28 days days
infectious and non infectious complications 28 days patients %
Trial Locations
- Locations (1)
asmaa Mostafa
🇪🇬Luxor, Egypt