Cardiogenic Shock Clinical Trials

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Cardiogenic Shock Integrated PHenotyping for Event Reduction

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

The purpose of this study is to better understand the time course of different biological mechanisms involved in acute decompensated heart failure complicated by cardiogenic shock throughout the evaluation of changes and the relationship among markers of inflammation (IL-6) and markers of increased endothelial permeability (Ang-2) or endothelial glycocalyx perturbation (Syndecan-1 and HS) and throughout a targeted metabolomic approach.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 74
View:

• Age ≥ 18 and \< 75, men and women;

• 1\) Systolic blood pressure (SBP) \< 90mmHg or mean arterial pressure (MAP) \< 60 mmHg, after an appropriate fluid challenge if there is no sign of overt fluid overload; OR 2) need of vasoactive agents to maintain SBP \> 90 mmHg or MAP \> 60 mmHg.

• Reduced ejection fraction (left ventricle systolic function ≤35%).

• Moreover, eligible patients have to fit at least ONE of the following criteria/items of overt hypoperfusion: altered state of consciousness; sweaty and cold skin; mixed venous oxygen saturation \< 60%; arterial lactates \> 2 mmol/L; oliguria \< 0.5 ml/Kg/h for at least 6 hours.

• Eligible patients shouldn't have contraindications to heart replacement therapy (HRT).

Locations
Other Locations
Italy
Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda
RECRUITING
Milan
Contact Information
Primary
Nuccia Morici, MD
nuccia.morici@ospedaleniguarda.it
+39026444
Backup
Alice Sacco, MD
alice.sacco@ospedaleniguarda.it
+39026444
Time Frame
Start Date: 2020-06-30
Estimated Completion Date: 2028-03-01
Participants
Target number of participants: 26
Treatments
Acute decompensated heart failure
patients admitted with Acute decompensated heart failure Complicated by cardiogenic shock
Sponsors
Leads: Niguarda Hospital

This content was sourced from clinicaltrials.gov