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Effects of compression of front of chest on mechanically ventilated patients with breathing machine

Effects of anterior chest wall compression on mechanically ventilated patients

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12622001392752
Enrollment
10
Registered
2022-10-31
Start date
2022-12-12
Completion date
Unknown
Last updated
2022-11-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Hypothesis of this study is application of anterior chest wall compression on mechanically ventilated patients will prevent ventral lung overdistention. We aim to examine changes in respiratory system compliance, oxygenation, ventilation and CT changes in lungs after applying anterior chest wall compression in mechanically ventilated patients We intend to enrol 10 patients in this single centre study. This trial will be conducted in the Southern Adelaide Local Health Network, Intensive and Critical Care Unit, Flinders Medical Centre. Screening and Recruitment Patients will be referred by treating ICU clinicians. Referral will be made as soon as possible after admission for patients who are intubated and ventilated Consent will be sought prior to enrolment Intervention Patient will have a 100 gm/kg weight placed on the anterior chest wall, while in supine position. The weight will be placed on the patients’ chest wall for 10 minutes and then removed. A number of measurements will be recorded before and after the procedure. Similar intervention repeated during CT chest. Device: weight on the anterior chest of the patient (soft and smooth weight (saline bags) placed and secure around each hemithorax) After enrolment, each patient will be treated as follows: Patients will be sedated and paralysed while mechanical ventilation settings will be kept unchanged over the course of the entire study. Initial baseline in the lying on the back ( Supine) position (T0) 10-minute period in supine position with 100 gm/kg soft and smooth weight (saline bags) placed and secure around each hemithorax (T1) In case of drop of oxygen level ( SPO2) , increase in delivered oxygen ( FiO2) will be allowed to achieve the previously described oxygen target. During the study, each patient will undergo standard ICU monitoring:

Interventions

Patient will have a 100 gm/kg weight placed on the anterior chest wall, while in supine position. The weight will be placed on the patients’ chest wall for 10 minutes and then removed. A number of measurements will be recorded before and after the procedure. Similar intervention repeated during CT chest. Device: 100 gm/kg soft and smooth weight (saline bags) placed and secure around each hemithorax Member of study team will be delivering the intervention. The period between the first session o

Patient will have a 100 gm/kg weight placed on the anterior chest wall, while in supine position. The weight will be placed on the patients’ chest wall for 10 minutes and then removed. A number of measurements will be recorded before and after the procedure. Similar intervention repeated during CT chest. Device: 100 gm/kg soft and smooth weight (saline bags) placed and secure around each hemithorax Member of study team will be delivering the intervention. The period between the first session of study and the CT session will be at least 1 hour. The total amount of time involved per session for all measurements and procedure to be completed would be around 1 hour.

Sponsors

Flinders Medical Centre
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Inclusion Patients who are 18 years or older admitted to the ICU at Flinders Medical Centre who have been identified as either of the following 1. Intubated and ventilated 2. PaO2/FiO2 greater than or equal to 300 with PEEP less than or equal to 5

Exclusion criteria

1. History of chronic respiratory condition (COPD/Interstitial lung disease) or any suspected lung infection 2. Current lung collapse, pleural effusion, pneumothorax, pulmonary embolism, chest trauma 3. Chest drain 4. Unstable spine, femur or pelvic fractures 5. Cardiovascular unstable -MAP < 65 mmHg despite ongoing high vasopressor /inotropic support, arrhythmias 6. Recent cardiothoracic surgery ( 4 weeks) 7. Patients who are admitted to ICU with active palliation 8. Admitted consultant is not happy for the patient to be enrolled in this study 9. Intracranial pressure > 20 mmHg or Cerebral perfusion pressure < 60 mmHg 10. Pregnant women

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026