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Fluid management strategies and outcomes in septic shock patients based on vascular leakage grading principles

Fluid management strategies and outcomes in septic shock patients based on vascular leakage grading principles

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500106271
Enrollment
Unknown
Registered
2025-07-21
Start date
2025-08-05
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sepsis

Interventions

Sepsis(septic shock) cohorts:None

Sponsors

Xiangya Hospital Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: PART1: 1.The field "Diagnosis Name" contains any of the following terms:"sepsis OR septicemia OR septic shock OR infectious shock OR bloodstream infection OR bacteremia"?? 2.?"Age at Visit" >= 18 years old? 3."Visit Date" is between 2021-01-01 and 2024-04-04? 4.The field "Order Content" contains the term:"intensive care" OR "critical care"?? PART2: 1.Age >= 18 years; 2.ICU stay time > 24h; 3.With the consent of patients or their authorized agent, and signed informed consent. PART3: ?1.Diagnosis:Meets ?Sepsis-3 septic shock diagnostic criteria:(1)Confirmed sepsis (life-threatening organ dysfunction with SOFA score increase >=2 due to infection);(2)Requires vasopressors to maintain ?MAP >=65 mmHg? despite adequate fluid resuscitation;(3)Serum lactate >2 mmol/L?. ?2.Age: ?18–80 years old, both sexes eligible 3.With the consent of patients or their authorized agent, and signed informed consent.

Exclusion criteria

Exclusion criteria: PART1: 1.Missing ?key prognostic data? affecting statistical validity. PART2: 1.Patients with cutaneous lesions (e.g., ulcers, rashes), burns, or active bleeding at the ultrasound measurement site; 2.Patients unable to cooperate due to delirium, agitation, or other behavioral disturbances. PART3: 1.Patients with recurrent sepsis episodes ("second-hit" phenomenon) during disease course; 2.Planned surgical/interventional procedures within 24h post-enrollment that may compromise fluid therapy data quality; 3.Scheduled ECMO initiation within 72h before/after enrollment; 4.Other investigator-determined exclusionary conditions.

Design outcomes

Primary

MeasureTime frame
Ultrasound strain elastography image index;Soft-hard area ratio;28-day all-cause mortality;

Secondary

MeasureTime frame
Liquid intake and output volume;Infusion duration of vasoactive drugs;

Countries

China

Contacts

Public ContactLina Zhang

Xiangya Hospital, Central South University

zln7095@163.com+86 158 7487 5763

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026