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NCT05692011

AN69ST Verse PS in CBP in Septic Children

Recruiting now Last updated 17 February 2026
What this trial tests

trial testing blood purification(PS) in Sepsis in 80 participants. Currently enrolling.

Timeline
1 October 2025
Primary endpoint
31 December 2026
31 December 2026

Quick facts

Lead sponsorChildren's Hospital of Fudan University
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment80
Start date1 October 2025
Primary completion31 December 2026
Estimated completion31 December 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Children's Hospital of Fudan University

Who can join

Adults 29 Days to 28, any sex, with Sepsis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In septic shock, dysregulated host responses to pathogens lead to cytokine storms that damage host tissues and organs, further contributing to the development of organ dysfunction and increased mortality. For sepsis, blood purification can remove inflammatory factors in sepsis by filtration or adsorption, so as to achieve the purpose of reducing inflammatory mediators in the body. However, there are few prospective randomized controlled studies in children. Therefore, this study intends to compare the efficacy and prognosis of different membrane on children with sepsis through a perspective cohort study, so as to provide a corresponding basis for the treatment of children with sepsis blood purification.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Sepsis

Currently open trials in the same condition.

Other Children's Hospital of Fudan University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05692011.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing