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Evaluation of the efficacy of continuous renal replacement therapy combined with blood adsorption in rhabdomyolysis with acute kidney injury: a single-center randomized controlled clinical trial

Evaluation of the efficacy of continuous renal replacement therapy combined with blood adsorption in rhabdomyolysis with acute kidney injury: a single-center randomized controlled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092176
Enrollment
Unknown
Registered
2024-11-12
Start date
2024-11-24
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

Rhabdomyolysis

Interventions

CRRT+HA group:Based on the CRRT group, the hemoperfusion device HA380 (Jianfan Biology, China) was connected in series after the filter for 10 hours.
CRRT group:The dialyzer uses AN69-ST150 membrane (Baxter Kinbao, USA), and the dialysis mode is CVVHDF. It is diluted and infused with commercial calcium-containing hemofiltration basic replacement fl

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.The patient meets the RM diagnostic criteria (creatine kinase > 1000 IU/L or more than 5 times the upper limit of normal, accompanied by a significant increase in serum myoglobin), and the patient's creatine kinase is >=5000IU/L, and myoglobin is >=3000ng/mL; 2. Diagnostic criteria for AKI: An increase of more than 26.5 µmol/L in serum creatinine within 48 hours or more than 50% of the baseline value within 7 days; Or urine output is less than 0.5 mL/ (kg·h) for more than 6 hours; 3. The clinical assessment indicates that the patient's condition requires continuous renal replacement therapy, and the patient or their family is willing to undergo CRRT or CRRT+HA treatment and sign the informed consent form. 4. RM patients with AKI who were admitted to the ICU.

Exclusion criteria

Exclusion criteria: 1. Those who have already received other blood purification treatment modes or plan to receive other blood purification treatment modes before enrollment; 2. The cause of the patient's rhabdomyolysis is myositis or myopathy. 3. Have a history of chronic renal insufficiency; 4. Pregnant women and patients who have undergone organ transplants; 5. Patients or their family members who are unwilling to participate in this trial.

Design outcomes

Primary

MeasureTime frame
Myoglobin plasma clearance ;

Secondary

MeasureTime frame
Creatine kinase plasma clearance ;Haemodynamics;Recovery of renal function;All-cause mortality;APACHE II score and SOFA score;Length of hospital stay;Plasma Clearance Efficiency of Myoglobin and Creatine Kinase by Blood Adsorption;

Countries

China

Contacts

Public ContactLing Zhang

West China Hospital of Sichuan University

zhangling_crrt@163.com+86 189 8060 1985

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026