Skip to content

Clinical efficacy of percutaneous phrenic nerve-abdominal muscle electrical stimulation in patients with severe pneumonia

Clinical efficacy of percutaneous phrenic nerve-abdominal muscle electrical stimulation in patients with severe pneumonia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125106
Enrollment
Unknown
Registered
2026-05-21
Start date
2026-05-24
Completion date
Unknown
Last updated
2026-05-25

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

Conditions

Severe pneumonia

Interventions

Experimental group:Transcutaneous phrenic nerve and abdominal muscle electrical stimulation
Control group:Conventional treatment

Sponsors

The First Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Meet the diagnostic criteria for severe pneumonia according to the 2019 American Thoracic Society and Infectious Diseases Society of America clinical practice guideline for the diagnosis and treatment of adults with community-acquired pneumonia. 2.Aged 40 to 80 years. 3.Provide signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Women who are pregnant or lactating. 2. Presence of unhealed wounds, active infection, or skin breakdown in the neck, upper chest, or abdominal area. 3. Bleeding tendency or coagulation dysfunction (confirmed by clinical assessment or laboratory tests indicating significant bleeding risk, such as platelet count 3 times the upper limit of normal, eGFR = III, or other conditions judged by the investigator to pose significant risks). 5. Presence of an implanted cardiac pacemaker, implantable cardioverter-defibrillator (ICD), or other electronic implantable devices. 6. Unhealed wounds after thoracic or abdominal surgery. 7. Individuals with reduced skin sensation, impaired skin perception, or skin abnormalities (e.g., easily irritated skin, local skin damage, infection, scar hyperplasia affecting electrode placement). 8. Severe cognitive impairment that precludes cooperation with treatment, unconsciousness, joint contracture deformities of the limbs, or severe contracture deformities due to osteoarthritis. 9. Presence of metal implants in the eyes, cardiac region, or carotid sinus area, or local lesions requiring avoidance of electrical stimulation. 10. Inability to provide informed consent, or deemed unsuitable for participation by the investigator.

Design outcomes

Primary

MeasureTime frame
Blood gas parameters;Clinical Pulmonary Infection Score;Inflammatory markers;Oxygenation index;

Secondary

MeasureTime frame
Rapid Shallow Breathing Index;Mortality rate;Duration of mechanical ventilation during ICU stay;Length of ICU stay;

Countries

China

Contacts

Public ContactFeng Min

The First Affiliated Hospital of Dalian Medical University

fengmin@firsthosp-dmu.com+86 411 8363 5963

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 30, 2026