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NCT06666946: SEPSIS-ACU

Efficacy and Safety of Electroacupuncture for ICU Sepsis Patients

Recruiting now NA Last updated 18 April 2025
What this trial tests

NA trial testing Electroacupuncture in Sepsis in 308 participants. Currently enrolling.

Timeline
11 February 2025
Primary endpoint
1 August 2026
31 August 2026

Quick facts

Lead sponsorShusheng Li
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment308
Start date11 February 2025
Primary completion1 August 2026
Estimated completion31 August 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shusheng Li

Who can join

18 and older, any sex, with Sepsis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the efficacy and safety of electroacupuncture (EA) combined with standard Intensive Care Unit (ICU) therapy on organ dysfunction and other clinical outcomes in sepsis patients. Additionally, this study will conduct subgroup analyses to investigate the influence of septic shock and immunomodulators on the treatment effects and their correlation with electroacupuncture efficacy.

Publications & conference data

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

  1. Advances in Medical Devices for Augmented Acupuncture Therapy.
    Cai R, Yu C, Luo X, Xu N, et al · · 2025 · cited 1× · PMID 40679074 · DOI 10.1002/advs.202505318

Verify or expand the search:

Other trials of Electroacupuncture

Trials testing the same drug.

Other recruiting trials for Sepsis

Currently open trials in the same condition.

Other Shusheng Li 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/NCT06666946.

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