Critical Illness Clinical Trial
Official title:
Intrarenal Venous Flow Change During Fluid Removal in Critically Ill Patients: A Prospective Exploratory Study
This clinical trial aims to study intrarenal venous flow patterns change during fluid removal treatment in critically ill patients
Status | Recruiting |
Enrollment | 52 |
Est. completion date | February 28, 2025 |
Est. primary completion date | February 28, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. Adult patients aged 18 years old or older who will be admitted to the medical intensive care unit 2. Expected to be hospitalized in the intensive care unit for more than 120 hours. 3. The patient has stable vital signs without the need for vasoactive medications or rapid fluid resuscitation (at least 500 milliliters of colloid or 1000 milliliters of crystalloid via rapid intravenous infusion) for a minimum consecutive period of 12 hours. This includes cases where the patient receives norepinephrine at a rate not exceeding 0.1 micrograms per kilogram per minute and dobutamine at a rate not exceeding 10 micrograms per kilogram per minute, or when the patient can maintain a continuous reduction in vasoactive medications for a minimum consecutive period of 12 hours. 4. The patient does not exhibit signs suggestive of inadequate organ perfusion, such as mottling skin, a capillary refill time of more than 2 seconds when nailbeds are pressed and released, or cold extremities. 5. The patients require fluid removal through decisions made by attending staff or clinical guidelines, which may involve the administration of diuretics or Renal Replacement Therapy. Exclusion Criteria: 1. Underlying chronic kidney disease (eGFR< 30) before enrollment 2. Chronic renal replacement therapy (RRT) before enrollment such as on intermittent hemodialysis, peritoneal dialysis 3. Decompensated cirrhosis with portal hypertension 4. Inferior vena cava, portal vein, hepatic, renal vein thrombosis 5. Ureteral obstruction 6. Intraabdominal hypertension (Intraabdominal pressure > 12 mmHg) 7. Previous allergic or anaphylactic to diuretic 8. Pregnant women 9. Transplanted kidney, transplanted liver 10. Patients with do-not-resuscitate (DNR) orders or decisions to withhold life-sustaining treatments 11. Patients or their legally authorized representatives (LAR), who decline participation in the study or are unable to provide informed consent before enrollment |
Country | Name | City | State |
---|---|---|---|
Thailand | Siriraj Hospital, Mahidol University | Bangkok Noi | Bangkok |
Lead Sponsor | Collaborator |
---|---|
Mahidol University |
Thailand,
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* Note: There are 16 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | intrarenal venous flow patterns change during fluid removal treatment in critically ill patients. | intrarenal venous flow patterns change measured by ultrasonography | 72 hours after Fluid removal therapy | |
Secondary | VExUS score change following fluid removal treatment in critically ill patients. | VExUS score change measured by ultrasonography | 72 hours after Fluid removal therapy |
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