Fluid Intolerance Signals as Safety Limits to Prevent Fluid-induced Harm During Septic Shock Resuscitation
Recruiting
N/A
Interventional Study
Septic Shock
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 100
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 62 (estimated)
- Sponsor
- Pontificia Universidad Catolica de Chile · Other
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About This Trial
The goal of this multicentric randomized controlled trial is to compare, in septic shock patients who require further fluid resuscitation, two strategies of administering fluids. The intervention group will integrate fluid intolerance signals to the decision making process, while the control group will follow standard of care, for a 6 hour study protocol. The main question it aims to answer is
1.…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Diagnosed or suspected septic shock
* \< 24 hours since diagnosis
* Hypoperfusion signal (altered arterial lactate or CRT) that requires further resuscitation
* Mechanical ventilation
* Positive fluid responsiveness status
Exclusion Criteria:
* Pregnancy
* Do-not-resuscitate…
Contacts