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Transcutaneous auricular vagus nerve stimulation in intervention of sepsis induced myocardial dysfunction

Transcutaneous auricular vagus nerve stimulation in intervention of sepsis induced myocardial dysfunction

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085501
Enrollment
Unknown
Registered
2024-06-11
Start date
2024-06-28
Completion date
Unknown
Last updated
2024-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

sepsis induced myocardial dysfunction

Interventions

sham transcutaneous auricular vagus nerve stimulation (sham taVNS):Wear an transcutaneous auricular vagus nerve stimulator, but do not give electrical stimulation
transcutaneous auricular vagus nerve stimulation (taVNS):Transcutaneous Auricular vagus nerve stimulation

Sponsors

Qilu Hospital of Shandong University (Qingdao)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Voluntarily sign informed consent; 2. Adult patients (=18 years old); 3. No gender restriction; 4. Patients diagnosed with sepsis, echocardiography within 24 hours of sepsis diagnosis indicated LVEF < 50%.

Exclusion criteria

Exclusion criteria: 1. Previous history of myocardial ischemia, atrial fibrillation or valvular heart disease; 2. Patients suspected with acute coronary syndrome; 3. Patients with implanted devices (such as cardiac defibrillators or pacemakers); 4. Ear skin disease or infection; 5. Pregnant or breastfeeding; 6. Patients who are unable to stay still during treatment (such as epilepsy or Parkinson's disease); 7. Palliative care or clinician judgment that the patient is expected to die within 72 hours.

Design outcomes

Primary

MeasureTime frame
Left ventricular ejection fraction;

Secondary

MeasureTime frame
Echocardiography LVESD, LVEF, LVEDD, LVEDV, and LVESV;Serum levels of NT-proBNP, cTn I, CKMB and MYO, and serum levels of inflammatory factors;SOFA score and APACHE II score;The dosage of vasoactive drugs and the amount of crystal/colloidal fluids used for resuscitation;28 day mortality;ICU stay;heart rate variability;

Countries

China

Contacts

Public ContactWu Zhiyang

Qilu Hospital of Shandong University (Qingdao)

wzy838983646@126.com+86 185 6181 2387

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026