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NCT05652179

SGB Reduces the Incidence and Severity of CSA-AKI

Completed NA Last updated 23 January 2025
What this trial tests

NA trial testing Stellate ganglion block in Stellate Ganglion Block in 396 participants. Completed in 30 December 2023.

Timeline
10 January 2023
Primary endpoint
1 December 2023
30 December 2023

Quick facts

Lead sponsorYangzhou University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment396
Start date10 January 2023
Primary completion1 December 2023
Estimated completion30 December 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Yangzhou University

Who can join

Adults 18 to 80, any sex, with Stellate Ganglion Block. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The incidence of acute kidney injury after cardiopulmonary bypass cardiac surgery is high, which increases postoperative mortality and is not conducive to the prognosis of patients. Stellate ganglion blocks increase renal blood flow, reduce inflammation and stress, and protect the heart muscle. In this study, stellate ganglion block was used to promote rapid recovery of kidney function after cardiopulmonary bypass cardiac surgery.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Preemptive left stellate ganglion block reduces the incidence and severity of cardiac surgery-associated acute kidney injury: a randomized clinical trial.
    Zhou W, Yu Y, Tian S, Wu H, et al · · 2025 · cited 2× · PMID 40643258 · DOI 10.1097/js9.0000000000002913

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Other trials of Stellate ganglion block

Trials testing the same drug.

Other recruiting trials for Stellate Ganglion Block

Currently open trials in the same condition.

Other Yangzhou University trials

Trials by the same sponsor.

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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/NCT05652179.

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