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A non-inferior, randomized trial compares low-dose and conventional-dose intensity of continuous renal replacement therapy in critically ill patients with acute kidney injury

A non-inferior, randomized trial compares low-dose and conventional-dose intensity of continuous renal replacement therapy in critically ill patients with acute kidney injury (CONDENSE-AKI)

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250624008
Enrollment
490
Registered
2025-06-24
Start date
2025-06-05
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Continuous renal replacement therapy Critically ill patients with acute kidney injury Continuous renal replacement therapy Critically ill patients Acute kidney injury

Interventions

CRRT at dose of 20-25 ml/kg/h,CRRT at dose of 10-15 ml/kg/h
Active Comparator Drug,Active Comparator Drug

Sponsors

No
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Critically ill patients with acute kidney injury who require CRRT in medical or surgical intensive care unit and have received CRRT for more than 48 hours, along with the following criteria: a. pH greater than or equal to 7.25 b. Serum potassium less than or equal to 6 mmol/L c. BUN less than or equal to 100 mg/dL 2. Aged greater than or equal to 18 years.

Exclusion criteria

Exclusion criteria: 1. Chronic kidney disease stage 5 2. Pregnancy 3. Patients with history of allergic reaction to filter used for renal replacement therapy 4. Patients who receive intermittent hemodialysis, sustained low-efficiency daily dialysis, or peritoneal dialysis 5. Patients anticipated to have a life expectancy of less than 48 hours 6. Terminally ill patients or patient refuse to treatment 7. Require standard or high dose CRRT after initiate CRRT more than 48 hours

Design outcomes

Primary

MeasureTime frame
Renal replacement therapy free-day Day 30 post-enrollment Renal replacement therapy free-day at day 30,Renal replacement therapy dependence Day 30 post-enrollment Renal replacement therapy dependence at day 30

Secondary

MeasureTime frame
Survival rate Day 30 post-enrollment Survival rate at day 30,Rate of renal recovery Day 30 post-enrollment Rate of renal recovery at day 30,Major Adverse Kidney Event at day 30 (MAKE 30) Day 30 post-enrollment Major Adverse Kidney Event at day 30 (MAKE 30),Vasopressor-free days Day 30 post-enrollment Vasopressor-free days at day 30,Ventilator-free days Day 30 post-enrollment Ventilator-free days at day 30,ICU length of stay Until ICU discharge ICU length of stay,ICU mortality Day 30 post-enrollment ICU mortality,Hospital mortality Day 30 post-enrollment Hospital mortality,Hospital length of stay Until hospital discharge Hospital length of stay,Efficacy of metabolic control OD until day 3 Serum electrolytes levels,Adverse events Until day 30 post-enrollment Severe metabolic imbalance

Countries

Thailand

Contacts

Public ContactThummaporn Naorungroj

Division of Critical Care, Department of Medicine, Siriraj Hospital, Mahidol University

thummaporn.nao@mahidol.ac.th0817365788

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026