800-Patient registry aims to unlock secrets of heart shock survival
NCT ID NCT07597291
First seen May 23, 2026 · Last updated Jun 22, 2026 · Updated 3 times
Summary
This observational study follows 800 adults admitted to a cardiology department with cardiogenic shock, a life-threatening condition where the heart suddenly can't pump enough blood. Researchers will review medical records from 2017 onward to see how treatments and survival rates have changed. Participants receive standard care, and their data is collected for up to one year. The goal is to identify which management strategies lead to better outcomes.
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This is a summary of
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Study contacts
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Contact
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Locations
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Unidade Local de Saúde de Lisboa Ocidental
RECRUITINGCarnaxide, Lisbon District, 2790-134, Portugal
Contact
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What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
What this could lead to
If successful, this registry could reveal which management strategies improve survival for cardiogenic shock patients.
What could go wrong
This is an observational study, not a treatment trial. It cannot prove cause and effect, and results may not apply to all hospitals or patients.
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.