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Improvement of Lung and Thoracic Compliance in ARDS Patients in Prone Position by Using Inflatable Air Bag

Improvement of Lung and Thoracic Compliance in ARDS Patients in Prone Position by Using Inflatable Air Bag

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05515484
Acronym
MAPIC
Enrollment
30
Registered
2022-08-25
Start date
2022-08-23
Completion date
2025-08-31
Last updated
2025-05-28

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

Conditions

Airbag, ARDS, Mechanical Ventilation, Prone Position

Keywords

ARDS, prone position, mechanical ventilation, airbag

Brief summary

ARDS is frequent in ICU and may lead to many complications and to death. Prone position is widely used in ADRS patients and demonstrated to decrease mortality. Regarding the chest wall compliance data are missing but the theorical response is that this compliance is decreased in a prone position mainly due to anterior chest and abdomen compression in this position which are more compliant that dorsal part of the body. As well prone position could be associated with complications as pressure ulcers. Because prone position is associated with complications, air bag were developped to decrease pressure on the chest and abdomen and to decrease pressure ulcers. Then, trying to improve chest compliance in prone position and reducing the risk of pressures ulcers could be a challenge with this system in comparison with standard care.

Interventions

OTHERprone position with airbags

prone position with airbags

OTHERprone position without airbags

prone position without airbags

Sponsors

Centre Hospitalier Universitaire, Amiens
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* patients with ARDS under mechanical ventilation with P/F ratio\<150 * Age \>18 y/o * Admitted in the medical ICU of Amiens under mechanical ventilation sedated, * With signed informed consent (patient or relative if patient is not conscious)

Exclusion criteria

* patients not eligible for a prone position * Patients with tracheostomy

Design outcomes

Primary

MeasureTime frame
variation of Lung compliance between both groups3 days

Countries

France

Contacts

Primary ContactPr Michel Slama, Pr
slama.michel@chu-amiens.fr0322087841

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026