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NCT07062744

The Role of Swan-Ganz Catheter in Hemodynamic Resuscitation for Patients With Cardiogenic Shock

Recruiting now NA Last updated 14 July 2025
What this trial tests

NA trial testing Swan-Ganz IQ Pulmonary Arterial catheter in Cardiogenic Shock in 108 participants. Currently enrolling.

Timeline
27 May 2025
Primary endpoint
1 December 2027
30 December 2027

Quick facts

Lead sponsorBach Mai Hospital
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment108
Start date27 May 2025
Primary completion1 December 2027
Estimated completion30 December 2027
Sites1 location across Vietnam

Drugs / interventions tested

Conditions studied

Sponsor

Bach Mai Hospital

Who can join

18 and older, any sex, with Cardiogenic Shock or Pulmonary Artery Catheter Waveform Interpretation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This clinical trial examines whether the use of the Swan-Ganz catheter, a specialized pulmonary artery catheter, can improve hemodynamic management and treatment outcomes in patients experiencing cardiogenic shock due to acute myocardial infarction (AMI). Cardiogenic shock is a critical condition marked by the heart's inability to supply adequate blood to the organs, often resulting from a severe heart attack. Despite advancements in care, the condition remains associated with high mortality. Effective monitoring of cardiovascular status is crucial in guiding timely and tailored treatment decisions. Participants in this study will undergo advanced hemodynamic monitoring using the Swan-Ganz catheter, which provides continuous data on cardiac output and other key parameters. This information enables physicians to better assess circulatory function and adjust therapies accordingly. The research will evaluate clinical characteristics, response to treatment, and 30-day outcomes in patients managed with this technique. The study also aims to identify factors associated with successful hemodynamic stabilization and potential complications related to catheter use. A total of 108 adult patients meeting specific eligibility criteria will be enrolled at Bach Mai Hospital over 3 years. Participation is voluntary, and all patients will continue to receive standard-of-care treatment. All personal and medical data will be handled with strict confidentiality.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Cardiogenic Shock

Currently open trials in the same condition.

Other Bach Mai Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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