Protocolized Reduction of Non-resuscitation Fluids Versus Usual Care in Septic Shock Patients

Recruiting N/A Interventional Study
Septic Shock
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
1,850 (estimated)
Sponsor
Region Skane · Other
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About This Trial

The objective of this trial is to assess the beneficial and harmful effects of a restrictive strategy for administration of non-resuscitation fluids in adult patients with septic shock.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adult (≥ 18 years of age) * Septic shock according to the Sepsis 3 criteria at any time within 12 hours after ICU admission (suspected or confirmed infection, plasma lactate above 2 mmol/L, and infusion of vasopressor/inotrope to maintain mean arterial pressure of 65mmHg or ab…
Contacts

Peter Bentzer

+46 42-4061111

Peter.Bentzer@med.lu.se

CONTACT

Jane Fisher

jane.fisher@advansci-research.com

CONTACT