Air Stacking Technique Efficacy on Peak of Expiratory Flow and Cough Peak Flow in Non-cardiac Thoracic Surgery
Air Stacking Technique Efficacy on Expiratory Peak of Expiratory Flow and Cough Peak Flow in Patients Undergoing Non-cardiac Thoracic Surgery
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
São Paulo, Brazil, 04115000
- Luciana Chiavegato
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients aged 18 years or older eligible for elective noncardiac intrathoracic surgery;
- Any gender;
- Clinically stable
- Able to perform study procedures.
Exclusion Criteria:
- Patients remained on mechanical ventilation for more than 72 hours at the PO;
- Rib fracture
- Rehospitalization in the ICU or readmission to the intensive care unit (ICU);
- Lowed level of consciousness, nausea and vomiting;
- Hemodynamic instability;
- New surgical intervention before the 3rd.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Air staking technique group
The air staking group
|
To perform the air stacking technique, an air manual breathing unit (AMBU) was used, attached to a unidirectional valve and nasal/oral mask.
For each AMBU manual compression (three in the total), the patient was instructed to breathe in deeply and hold the air inside the lungs.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Peak of expiratory flow (PEF)
Time Frame: pre operative and 3th postoperative day ( pre and pos air stacking application)
|
PEF was measured with a peak flow meter ranging from 100 to 900 L/min (Philips Respironics®) following the literature recommendations.
The patient remained seated at 90º with a nasal clip and was asked to force maximum expiration as fast as he could through the mouthpiece after maximum inspiration to measure PEF
|
pre operative and 3th postoperative day ( pre and pos air stacking application)
|
|
Cough peak flow (CPF)
Time Frame: pre operative and 3th postoperative day ( pre and pos air stacking application)
|
CPF were measured with a peak flow meter ranging from 100 to 900 L/min (Philips Respironics®) following the literature recommendations.
The patient remained seated at 90º with a nasal clip and was asked to force maximum expiration as fast as he could through the mouthpiece after maximum inspiration to measure PEF.
To measure cough peak flow, the patient repeated the inspiratory maneuver and was asked to cough as hard as he could.
At least three measurements of both variables were performed
|
pre operative and 3th postoperative day ( pre and pos air stacking application)
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maximum Inspiratory Pressure ( MIP)
Time Frame: pre operative and 3th postoperative day ( pre and pos air stacking application)
|
MIP and MEP) were measured with a previously calibrated aneroid manovacuometer (GER-AR®), ranging from 5 to ± 300 cmH2O.
A mouthpiece was attached to the manovacuometer, and the nasal clip was used during the maneuvers following previous recommendations
|
pre operative and 3th postoperative day ( pre and pos air stacking application)
|
|
Maximun Expiratory Pressure (MEP)
Time Frame: pre operative and 3th postoperative day ( pre and pos air stacking application)
|
MIP and MEP) were measured with a previously calibrated aneroid manovacuometer (GER-AR®), ranging from 5 to ± 300 cmH2O.
A mouthpiece was attached to the manovacuometer, and the nasal clip was used during the maneuvers following previous recommendations
|
pre operative and 3th postoperative day ( pre and pos air stacking application)
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Investigators
Investigators
- Principal Investigator: Luciana D Chiavegato, PhD, Federal University of São Paulo
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- UNIFESP
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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