Clinical Implementation of the Use of Positive Pressure in Chest Drainage
NCT03896672 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 64
Last updated 2023-07-03
Summary
Background: Scientific evidence appoints that the use of non-invasive positive airway pressure in pleural effusion drainage patients is associated with a reduction in these complications, as well as with other benefits. Objectives: To test the implementation of the best evidence-based practices for the use of non-invasive continuous positive airway pressure (CPAP) in patients with chest drainage for pleural effusion, by acceptability, reach, appropriateness, direct costs, feasibility, fidelity, penetration, and sustainability. In addition, to assess the impact of implementing these practices on health-related outcomes of patients having their pleural effusion drained through dwelling time of the chest tube, hospital stay and others relevant outcomes. Methods: quasi-experimental study with pretest-posttest design. Eight hospitals that provide physiotherapeutic care to pleural effusion drainage patients will be involved. The study will be developed in three phases. In phase I, a audit team will help the local research team to elaborate strategies to cope with barriers related to the use of CPAP in patients with pleural effusion and catheter drainage, using a interview with the physical therapist, patient history analysis, and interviews with the patients. In implementation phase, the results obtained from phase I will be presented to physiotherapists to physiotherapists and a discussion will be started on the evidence regarding the best practices in the application of CPAP for educational purposes only. In phase III, new interviews will be held with the physical therapist and patients and the patient histories will be analyzed to assess the impact of the intervention 30 days after implementation phase.
Conditions
- Pleural Effusion
Interventions
- DEVICE
-
Continuous Positive Airway Pressure
Continuous Positive Airway Pressure will be applied three times daily during 7 consecutive days, if the physiotherapist follow the previous training. Each application should during 30 minutes. Pressure should be adjusted in 15 centimeters of water.
Sponsors & Collaborators
-
Universidade Cidade de Sao Paulo
lead OTHER
Principal Investigators
-
Adriana Lunardi, PhD · Universidade Cidade de São Paulo
Study Design
- Allocation
- NA
- Purpose
- OTHER
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 85 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-09-01
- Primary Completion
- 2021-01-31
- Completion
- 2023-01-31
Countries
- Brazil
Study Locations
More Related Trials
-
Measurement of Cardiac Output in Intensive Care Unit With Unstable Hemodynamic: Validation of Physioflow® Device Versus Trans Thoracic Echocardiography
NCT03937102 ·Status: COMPLETED
-
Assessment of Esophageal Pressure Reliability to Estimate Pleural Pressure in Critically Ill Children
NCT02762279 ·Status: COMPLETED ·Phase: NA
-
Acute Effect of Continuous Positive Airway Pressure in Heart Failure
NCT01088854 ·Status: COMPLETED ·Phase: PHASE2
-
Electrical Impedance Tomography: Collapse in Dependent Areas as a Predictor of Response to Prone Position Ventilation in COVID-19 Acute Respiratory Distress Syndrome
NCT04603755 ·Status: COMPLETED
-
Effects of PEEP on Heart and Lungs in Obese Subjects
NCT02523352 ·Status: UNKNOWN ·Phase: NA
-
PEEP Incremental and Decremental Alveolar Recruitment of Critically Ill Corona Virus Disease-19 (COVID-19) Patients
NCT04360837 ·Status: COMPLETED ·Phase: NA
-
Cuff Pressure Control and Evacuation of Subglottic Secretions To Prevent Pneumonia
NCT05403320 ·Status: COMPLETED ·Phase: NA
-
Cuff Leak Test and Airway Obstruction in Mechanically Ventilated ICU
NCT03372707 ·Status: COMPLETED ·Phase: NA
-
Determine the Effect of Prone Positioning in Adults With ARDS by Electrical Impedance Tomography
NCT04725227 ·Status: UNKNOWN
-
Ventilatory Monitoring in Children With Respiratory Distress Syndrome With Electrical Impedance Tomography
NCT03768921 ·Status: COMPLETED ·Phase: NA
-
Driving Pressure Guided VT in ARDS Patients
NCT05207267 ·Status: COMPLETED ·Phase: NA
-
Correlation of Survival in Puerperae by Electrical Impedance Tomography
NCT03715647 ·Status: COMPLETED
-
Comparison of Different Methods to Calculate Pendelluft by Electrical Impedance Tomography in Mechanically Ventilated Patients
NCT06494215 ·Status: RECRUITING ·Phase: NA
-
Physiological Behavior of Respiratory Maneuvers
NCT03270826 ·Status: COMPLETED
-
STUDY OF ELECTRICAL STIMULATION IN PULMONARY FUNCTION IN INTENSIVE CARE UNIT
NCT03712215 ·Status: COMPLETED ·Phase: NA
-
Physiological Effects of Lung Impedance Tomography-Guided and Plat Pressure-Guided Phigh During APRV in Patients With ARDS
NCT06696638 ·Status: RECRUITING ·Phase: NA
-
Electrical Impedance Tomography in Evaluating the Effects of Noninvasive Ventilation in Post-Operative Cardiac Surgery
NCT03371628 ·Status: UNKNOWN ·Phase: NA
-
Comparison of Two Strategies for Endotracheal Tube Cuff Underinflation Prevention During Invasive Mechanical Ventilation
NCT03330379 ·Status: COMPLETED ·Phase: NA
-
Inspiratory Muscle Therapy in Subjects With Fontan Circulations
NCT03339466 ·Status: COMPLETED ·Phase: NA
-
Thoracic Fluid Content in Prediction of Failure of Weaning From Mechanical Ventilation
NCT03094390 ·Status: COMPLETED
-
Determine the Effects of Prone Positioning and NO in COVID-19 ARDS by EIT
NCT05715762 ·Status: UNKNOWN
-
Transmitted Lung Pressures With Biphasic Chest Cuirass
NCT03799588 ·Status: WITHDRAWN ·Phase: NA
-
Assessment of Human Diaphragm Strength by Magnetic and Electric Stimulation After Ultrasonography Phrenic Nerve Tracking
NCT04199273 ·Status: COMPLETED ·Phase: NA
-
Assessment of Cough Strength in Patients With Tracheostomies
NCT02566512 ·Status: COMPLETED ·Phase: NA
-
Combining Electrical Impedance Tomography and Thoracic Ultrasound Toinvestigate Dynamic Changes
NCT06958770 ·Status: NOT_YET_RECRUITING