Actively Recruiting

Age: 28Days - 18Years
All Genders
ID04794595

Clinical Features and Outcomes of Continuous Blood Purification Versus Non-continuous Blood Purification in Pediatric Patients With Sepsis or Septic Shock

Led by Children's Hospital of Fudan University · Updated on 2026-03-16

90

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

C

Children's Hospital of Fudan University

Lead Sponsor

S

Shanghai Children's Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to explore the effects and timing of continuous blood purification (CBP) in children who have sepsis or septic shock. Sepsis can cause severe immune dysfunction and organ damage, and while CBP may help remove harmful inflammatory factors and support immune balance, the best timing for starting this treatment in children is not yet clear. The study focuses on understanding how early CBP intervention might improve outcomes in pediatric sepsis cases. Participants are divided into two groups: children with sepsis who should receive CBP but did not get it for various reasons, and those who were treated with CBP. CBP is a procedure used to manage fluid overload and organ dysfunction in septic children by removing cytokines and supporting kidney function, especially when other fluid management strategies are insufficient. The study observes these two groups to compare clinical features and outcomes. During the study, researchers will monitor children’s survival rates 28 days after hospital discharge as the main outcome. Secondary measures include creatinine levels in children who do not survive. The study involves regular assessments to track the effects of CBP on organ function and immune response. Participants’ progress is followed from the early treatment phase through discharge and up to 28 days afterward, to gather comprehensive data on treatment impact and prognosis.

CONDITIONS

Brief Title

Clinical Features and Outcomes of CBP Versus Non-CBP in Septic Children

Who Can Participate

Age: 28Days - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age of 29 days to 18 years old
  • Children diagnosed with sepsis requiring blood purification
Not Eligible

You will not qualify if you...

  • History of pediatric intensive care unit stay less than 24 hours
  • Active bleeding, including cerebral hemorrhage

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - 28 days after hospital discharge

Participants with sepsis are observed to evaluate clinical features and outcomes with or without continuous blood purification treatment.

Follow-up visits during hospitalization and up to 28 days post-discharge

Trial Site Locations

Total: 1 location

1

Children'S Hospital of Fudan University

Shanghai, Shanghai Municipality, China, 201102

Actively Recruiting

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Research Team

Y

YING JIAYUN

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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