Analyzing metabolic factors in patients with septic shock
Official title: Metabolic Cluster Analysis in Septic Shock Patients Undergoing Hemodynamic Resuscitation. A Multicenter Observational Study
Run by Corporacion Parc Tauli · NCT06500156 · Data updated 2026-11-12
This study looks at how giving fluids to patients with septic shock in the ICU affects their heart and metabolism to help find better treatment methods.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 120 (estimated) |
| Sponsor | Corporacion Parc Tauli Academic / other |
| Locations | 1 site (Sabadell, Barcelona) |
| Status | Recruiting |
| Started | May 1, 2024 |
| Main results expected | October 31, 2026 |
| Study ends | October 31, 2026 |
| Registry record updated | December 5, 2025 |
| Trial ID | NCT06500156 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults diagnosed with septic shock within 24 hours of ICU admission who are selected for a fluid challenge due to suspected tissue hypoperfusion.
✕Probably not a fit
Patients under 18 years old, those with uncontrolled hemodynamic instability, or those receiving continuous renal replacement therapies may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study focuses on patients diagnosed with septic shock within the first 24 hours of their ICU admission. Participants will be monitored using a cardiac output estimation system while undergoing a fluid challenge to assess hemodynamic and metabolic parameters. The study aims to gather data on the effects of fluid resuscitation on these patients, particularly in relation to tissue hypoperfusion indicators such as elevated lactate levels. The findings could help improve understanding of optimal resuscitation strategies in critical care settings.
Why it matters
Potential benefit: If successful, this study could lead to improved resuscitation protocols for septic shock patients, potentially enhancing survival rates.
How similar studies have gone: While similar studies have explored fluid resuscitation in septic shock, this specific approach focusing on metabolic cluster analysis is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: \- Septic shock patients within the first 24 hours of ICU admission, and selected by the attending physician for performing a fluid challenge (FC) due to suspected tissue hypoperfusion (elevated lactate and/or ScvO2 \< 70%). Exclusion Criteria: * Age under 18 years old * Uncontrolled hemodynamic instability, defined as the need for significant changes in vasopressor support (\> 10% from baseline dose) within the 15-minute period prior to, and/or during the administration of fluids. * Patients receiving continuous renal replacement therapies, since the CO values obtained from the thermodilution techniques might be potentially affected.
Where it's running
-
Hospital Universitari Parc Taulí
Sabadell, Barcelona, Spain Recruiting
Study contacts
- Study coordinator: Jaume Mesquida, MD
- Email: jaume.mesquida@gmail.com
- Phone: +34937231010
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Adjunctive Fludrocortisone in Septic Shock on Hydrocortisone
In septic shock, this trial tests whether adding fludrocortisone (50 mcg or 100 mcg daily) to hydrocortisone improves survival and recovery compared with placebo.
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Non-invasive hemodynamic guidance for sepsis care on medical wards
This trial tests whether guiding fluid and vasopressor therapy for sepsis using non-invasive hemodynamic measurements works better than standard care.
-
Reducing Endotoxin Burden in Septic Shock Patients on CRRT with the oXiris Filter
This trial tests whether using the oXiris hemofilter during continuous kidney replacement helps lower endotoxin levels in adults with septic shock who need CRRT.
-
Personalized Fluid Resuscitation in the Emergency Department
This pilot test checks if a quick, non-invasive stroke-volume assessment can help ED doctors tailor IV fluids for septic patients with low blood pressure.
-
Discordance between capillary refill time and oxygen use in septic shock
This study tests whether some septic shock patients can have a normal capillary refill time but still lack tissue oxygen use, to see if that mismatch relates to 28-day survival.
-
Targeting upper-normal magnesium to see if norepinephrine needs drop in septic shock
This trial tests whether keeping magnesium levels at the upper end of normal can reduce the amount and duration of norepinephrine needed in adults with septic shock.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.