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Prospective Study on Electrical Impedance Tomography (EIT) for Monitoring Respiratory Curve Synchrony in Patients with Heart Failure

Prospective Study on Electrical Impedance Tomography (EIT) for Monitoring Respiratory Curve Synchrony in Patients with Heart Failure

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112986
Enrollment
Unknown
Registered
2025-11-21
Start date
2025-11-05
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Heart Failure

Interventions

Gold Standard:Ultrasonographic Assessment
Index test:Electrical Impedance Tomography (EIT)

Sponsors

Fuwai Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-80 years. 2. Killip class II-IV. 3. Ability to breathe spontaneously and calmly, and to cooperate in following breathing training instructions. 4. Borg score for dyspnea >= 3. 5. Diaphragmatic excursion < 2 cm, as measured by diaphragmatic ultrasonography. 6. Intact chest wall skin. 7. Participants who can understand the study purpose, voluntarily participate and sign the informed consent form, and agree to comply with the protocol requirements to complete the examinations.

Exclusion criteria

Exclusion criteria: 1. Patients clinically assessed and planned for emergency surgery (e.g., infective endocarditis, acute coronary syndrome, cardiac tamponade, etc.). 2. Patients already supported with Intra-aortic Balloon Pump (IABP), Extracorporeal Membrane Oxygenation (ECMO), Continuous Renal Replacement Therapy (CRRT), or Left Ventricular Assist Device (LVAD) at the time of admission. 3. Presence of acute pulmonary edema (e.g., manifesting as orthopnea, coughing up pink, frothy sputum) or cardiogenic shock. 4. Implantation of a cardiac pacemaker or Implantable Cardioverter-Defibrillator (ICD). 5. Presence of severe cardiac arrhythmias (e.g., atrial fibrillation). 6. Chest wall deformity (e.g., severe scoliosis). 7. Poor diaphragmatic acoustic window, preventing adequate diaphragmatic assessment. 8. Co-existing other pulmonary diseases (e.g., COPD, pneumothorax) or diaphragmatic paralysis. 9. Pregnancy or lactation. 10. Severe obesity (Body Mass Index [BMI] >= 35). 11. Participants deemed by the investigator to have poor compliance and unlikely to complete the study as required

Design outcomes

Primary

MeasureTime frame
Agreement between EIT-derived diaphragmatic excursion and ultrasonographically measured diaphragmatic excursion;Agreement between EIT-derived diaphragmatic excursion and ultrasonographically measured diaphragmatic excursion;

Countries

China

Contacts

Public ContactYiyao Shi

Fuwai Hospital, Chinese Academy of Medical Sciences

shiyiyaosherry@163.com+86 155 4021 8858

Outcome results

None listed

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