Clinical Trials Directory

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RecruitingNCT07190079

Saline Contrast Electrical Impedance Tomography Method for Diagnosis of Acute Pulmonary Embolism

A Multicenter Comparative Study of Saline Contrast Electrical Impedance Tomography Method Versus CTPA in the Diagnosis of Acute Pulmonary Embolism

Status
Recruiting
Phase
Study type
Observational
Enrollment
343 (estimated)
Sponsor
Peking Union Medical College Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this observational study is to compare the consistency of saline contrast Electrical Impedance Tomography(EIT) method and Computed Tomography Pulmonary Angiography (CTPA) in diagnosing acute pulmonary embolism. The main question it aims to answer is: Can bedside saline contrast EIT method be used for the diagnosis of acute pulmonary embolism? The participants will undergo saline contrast EIT and CTPA examinations successively within 24 hours.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTSaline contrast Electrical Impedance Tomography methodThis study will enroll patients with clinically suspected or confirmed acute pulmonary embolism (PE) presenting with acute respiratory failure, who undergo electrical impedance tomography (EIT) with saline contrast within 24 hours before or after computed tomography pulmonary angiography (CTPA). The EIT procedure is performed as follows: 1. Breath-Hold Maneuver: (1)Spontaneous breathing patients: Supine position, instructed to hold expiration for ≥8 seconds. (2)Mechanically ventilated patients: Expiratory hold (\>8 sec) achieved via ventilator; deeper sedation will be applied when feasible to prolong breath-hold. 2. Venous Access: (1)Preferred: Central venous catheter (internal jugular or subclavian vein).(2)Alternative: Peripheral forearm vein (preferably the median cubital vein). 3. Contrast Administration:(1)Central venous route: 10 mL of 10% NaCl.(2)Peripheral venous route: 15 mL of 5% NaHCO₃.
DIAGNOSTIC_TESTComputed Tomography Pulmonary Angiography (CTPA)Patients who meet the inclusion criteria will undergo CTPA examination using conventional clinical diagnostic methods.

Timeline

Start date
2025-09-24
Primary completion
2027-05-01
Completion
2027-09-15
First posted
2025-09-24
Last updated
2025-10-02

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07190079. Inclusion in this directory is not an endorsement.