Informations générales (source: ClinicalTrials.gov)
" Effects of Continuous Anterior Chest Compression (CACC) & Comparision With Prone Position in ARDS Patients " The StrapVent Study "
Interventional
N/A
Assistance Publique - Hôpitaux de Paris (Voir sur ClinicalTrials)
avril 2022
juin 2023
02 mars 2026
The aim is to test the physiological effects of continuous anterior chest compression in
patients with severe to moderate ARDS.
Etablissements
| Les établissements d'Île-de-France ayant mis à jour leurs données Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| AP-HP Assistance publique - Hôpitaux de Paris | 27/12/2025 07:42:11 | Contacter | |||
| AP-HP - Hôpital Henri Mondor-Albert Chenevier | |||||
| Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
| AP-HP - Hôpital Henri Mondor-Albert Chenevier | Contact (sur clinicalTrials) | ||||
Critères
Tous
- Age ≥ 18 ans
- Intubated moderate and severe ARDS according to the Berlin definition (PaO2/FiO2
ratio <= 200 mmHg)
- The patent must be sedated and paralyzed
- Informed consent from patient or family members
Exclusion Criteria:
- Extracorporeal membrane oxygenation (ECMO)
- Pneumothorax
- Thoracic trauma during the last 3 months
- Refractory shock
- Contraindication to EIT monitoring (e.g. burns, pacemaker, thoracic wounds limiting
electrode belt placement)
- Pregnancy
- Any contra-indication to esophageal manometry (less than one month esophagus
surgery, bronchopleural or esotracheal fistula, latex allergy)
- No social care
- Adults under Guardianship, curatorship or protection of the court