Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 2:14 PM
Ignite Modification Date:
2025-12-24 @ 2:14 PM
NCT ID:
NCT07081295
Eligibility Criteria:
Inclusion Criteria:
* In need of lung perfusion assessment due to clinical condition
* With central venous catheter
Exclusion Criteria:
* Pregnant or breastfeeding females
* contraindications to the use of EIT (automatic implantable cardioverter defibrillator, chest wounds limiting electrode belt placement, implantable pumps, etc.)
* severe hyperchloremia (\>155 mmol/L)
* unable to tolerate breath-hold maneuver
* edema disease (nephrotic syndrome, cirrhotic ascites, congestive heart failure, etc.)
* Patients with severe hypernatraemia or hyperchloremia and severe hypertonicity
* Hypertension (\>160/100 mmHg), hypokalaemia (\> 3.5 mmol/L)
* Acute renal failure in oliguric stage, chronic renal failure with reduced urine output and poor response to diuretics
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
79 Years
Study:
NCT07081295
Study Brief:
Protocol Section:
NCT07081295