NCT07321405Not yet recruiting
Assessment of Cardiac Output and Stroke Volume in Septic Shock Patients
Non Invasive Hemodynamic Assessment of Cardiac Output and Stroke Volume in Septic Shock Patients
Source: ClinicalTrials.gov · Last updated 7 Jan 2026
Brief summary (registry, in English)
The aim of this research is to compare the accuracy and reliability of electrical cardiometry versus transthoracic echocardiography in measuring cardiac output and stroke volume in patients with septic shock, to evaluate the potential of EC as a non-invasive alternative for hemodynamic monitoring.
- Status (registry)
- Not yet recruiting
- Study type
- Observational
- Enrollment
- 100 (estimated)
- First submitted
- 24 Nov 2025
- Start date
- 1 Apr 2026
- Primary completion date
- 1 Jul 2027
- Lead sponsor
- Assiut University
- Diseases
- Stroke
- NCT number
- NCT07321405
What you commit to
- Study type: Observational
- Planned participants: 100
- From 1 Apr 2026 to the primary completion date, 1 Jul 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Age
- patients aged less than 18 years pregnant women cases suffering cardiac diseases (heart failure, arrhythmia, moderate, and severe valvular disease) patients with poor quality echocardiographic images and measurements
Who the study is looking for
- \-
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Assiut University hospital Coordinator of this site? Confirm its status | Asyut | Egypt | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.