- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04670939
Respiratory Physiotherapy in Mechanical Ventilation
the Effect of Respiratory Physiotherapy to Weaning in Invasive Mechanical Ventilation
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Respiratory physiotherapy is a treatment approach to increase ventilation and function in patients with acute and chronic problems and to reduce respiratory work and dyspnea.Airway cleaning techniques, lung volume-enhancing approaches, thoracic mobilization, positioning, breathing exercises and inhalation therapy are among the strategies used.
In patients with invasive MV support, respiratory physiotherapy is the position, tracheal cleaning and inhalation therapy when necessary. But breathing exercises are not indicated in the acute phase. In the process of weaning, inspiratory muscle training and breathing exercises can be used.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Mugla, Turkey, 48000
- Mugla Sıtkı Kocman University Reasearch and Treaninig Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- weaning period of patients in invasive mechanical ventilation
- patients in stable hemodynamic parameters
Exclusion Criteria:
- under 18 years old
- pregnant
- non-cooperative
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: SPT
|
diaphragmatic breathing exercise that used during weaning is the respiratory physiotherapy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
weaning success
Time Frame: 1-7 days
|
effect of respiratory physiotherapy as diaphragmatic exercise of weaning
|
1-7 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Compliance
Time Frame: 1-7 days
|
effect of diaphragmatic exercise on compliance, diaphragmatic movement
|
1-7 days
|
diaphragmatic movement
Time Frame: 1-7 days
|
effect of diaphragmatic exercise on diaphragmatic movement
|
1-7 days
|
arterial blood gas
Time Frame: 1-7 days
|
effect of diaphragmatic exercise on diaphragmatic movement
|
1-7 days
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Canan Gürsoy, Muğla Sıtkı Koçaman University, Training And Research Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SFT-CNN
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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