Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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27 November 2023 |
Main ID: |
NCT03009331 |
Date of registration:
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14/12/2016 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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Descriptive and Comparative Study of Respiratory Function in the Postoperative Cardiac Surgery Patient
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Scientific title:
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Descriptive and Comparative Study of Respiratory Function in the Postoperative Cardiac Surgery Patient |
Date of first enrolment:
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July 25, 2017 |
Target sample size:
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30 |
Recruitment status: |
Active, not recruiting |
URL:
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https://clinicaltrials.gov/ct2/show/NCT03009331 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Supportive Care. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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Sweden
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Contacts
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Name:
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Sven-Erik Ricksten, Professor |
Address:
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Telephone:
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Email:
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Affiliation:
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The Salgrenska Academy |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Signed informed consent
- Scheduled cardiac surgery (CABG or valve surgery)
- Cardiopulmonary bypass
Exclusion Criteria:
- Diagnose of obstructive or restrictive lung disease
- Medical therapy with bronchodilators
- Smoking or former smoking > 5 years
- Obesity (BMI > 30)
- Perioperative FiO2 >60% or PEEP >12
- Haemodynmic instability, use of inotropes (low dose vasopressors accepted)
- Postop clinically significant bleeding (>100 ml/h, reoperation)
- Postoperative haemothorax or large pleural effusion detected with ultrasonography
- Postoperative clinically significant pneumothorax or large chestdrain airleak
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Pulmonary Atelectasis
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Intervention(s)
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Procedure: Lungrecruitment manoeuver in prone position.
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Procedure: Lungrecruitment manoeuver in supine position.
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Primary Outcome(s)
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P/F ratio
[Time Frame: 5 days]
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Chest X-ray
[Time Frame: 5 days]
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Electrical impedance
[Time Frame: 5 days]
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Lungcompliance (ml/cm H2O)
[Time Frame: 2 hours]
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Ultrasonography
[Time Frame: 5 days]
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Secondary ID(s)
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AMartinssonthorax
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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