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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age28-18
SponsorChildren's Hospital of Fudan University

About this trial

The effect of continuous blood purification (CBP) in children is unclear. Also, the timing of early application is still being explored. In this study, we need to explore the efficacy and the timing of application of CBP in children with sepsis or septic shock.

Eligibility criteria

Qualifiers

Age of 29d to 18 years old;

Children diagnosed with sepsis requiring blood purification.

Disqualifiers

with a history of a duration of PICU stay <24 h

active bleeding, including cerebral hemorrhage

Trial design

Treatments tested in this trial

  • CBP

Treatment groups

90 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Children's Hospital of Fudan University

Lead sponsor

Shanghai Children's Hospital

Collaborator

Shanghai Children's Medical Center

Collaborator

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Collaborator