Comparison of Manual PAOP and Automatic PAOP (Smart Wedge)
ConditionSeptic Shock
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAssistance Publique - Hôpitaux de Paris
About this trial
The pulmonary artery catheter (Swan-Ganz) is a standard tool in intensive care for measuring and monitoring the pulmonary artery occlusion pressure (PAOP). The Swan-Ganz IQ™ model also allows automatic measurement to reduce the risk of error (Smart Wedge). However, the concordance between this automatic method and the manual method remains poorly studied in real clinical conditions and may vary depending on certain clinical situations. This study therefore aims to compare the PAOP automatically measured (Smart Wedge) with the manual PAOP measurement at bedside based on data collected in clinical practice.
Eligibility criteria
Qualifiers
Age ≥18 years;
Admission to an intensive care unit;
Presence of a Swan-Ganz IQ™ pulmonary artery catheter placed as part of patient care;
Measurement of pulmonary artery occlusion pressure (PAOP) performed by the attending clinician as part of patient care.
Disqualifiers
Pregnancy;
Court-ordered protective measures.
Refusal to participate by the patient's family members or the patient themselves.
Cardiac output measurements by thermodilution or by continuous cardiac output analysis that cannot be interpreted.
Trial design
Treatments tested in this trial
- Swan-Ganz IQ™, Smart Wedge
Treatment groups
No treatment groups listed
Locations
Sponsors and collaborators
Source ClinicalTrials.gov