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 @ 1:31 PM
Ignite Modification Date:
2025-12-24 @ 1:31 PM
NCT ID:
NCT05059795
Eligibility Criteria:
Inclusion Criteria:
1. Clinical/Imaging or Biopsy proven liver cirrhosis of any etiology
2. Hypotension (MAP \<65mmHg or SBP \<90mmHg)
3. 18-65 yrs of age
Exclusion Criteria:
1. Already received colloid or 2 litres of fluid within the first 2 hours of presentation, without echocardiographic assessment.
2. Already on vasopressors/inotropes
3. Severe pre-existing cardiopulmonary disease
4. Acute Respiratory Distress Syndrome (ARDS)
5. Active bleeding like variceal bleed 28
6. Cerebrovascular events
7. Chronic renal disease - End Stage Renal Disease (ESRD)/ patient on renal replacement therapy
8. Admission to ICU following liver transplantation, burns, cardiac surgery
9. Brain death or likely brain death within 24 hours
10. Previous adverse reaction to human albumin solution
11. Pregnant or lactating women
12. Informed consent refused by patient or attendants
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT05059795
Study Brief:
Protocol Section:
NCT05059795