Skip to content

High cut-off Continuous venovenous haemodialysis (CVVHD) to improve haemodynamic stability and Organ function scores in patients treated for acute renal failure after Systemic inflammatory response Syndrome (SIRS)/septic shock

High cut-off Continuous venovenous haemodialysis (CVVHD) to improve haemodynamic stability and Organ function scores in patients treated for acute renal failure after Systemic inflammatory response Syndrome (SIRS)/septic shock

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN77656437
Enrollment
120
Registered
2006-03-24
Start date
2004-02-04
Completion date
Unknown
Last updated
2019-05-05

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

Conditions

Acute renal failure after SIRS/septic shock Urological and Genital Diseases Renal failure

Interventions

Continuous venovenous haemodialysis treatment with high-flux or high-cut-off dialysers. Please note that as of 13/12/2007 the anticipated end date of this trial was extended to 31/12/

Sponsors

Gambro Dialysatoren GmbH (Germany)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Fulfilling at least two of the SIRS criteria as defined by the American College of Chest Physicians (ACCP)/Society of Critical Care Medicine (SCCM) Consensus Conference 2. Having signs of renal dysfunction 3. Requirement for catecholamine administration (norepinephrine or others) 4. Acute Physiology And Chronic Health Evaluation (APACHE II) score at enrolment greater than or equal to 19 and less than or equal to 30

Exclusion criteria

Exclusion criteria: 1. Lack of written informed consent from patients or a legally authorized surrogate 2. Duration of septic shock greater than 4 days 3. Hypoproteinaemia (characterized by serum albumin less than 18 g/l) 4. End stage renal failure 5. Known active malignancy 6. Known human immunodeficiency virus (HIV), hepatitis B virus (HBV) or hepatitis C virus (HCV) infection 7. Age younger than 18 years or older than 80 years 8. Known pregnancy 9. Immunosuppression after transplantation 10. Participation in another clinical study 11. Renal replacement therapy greater than 24 hours before randomisation

Design outcomes

Primary

MeasureTime frame
1. Dosage of vasopressors 2. Mean arterial pressure 3. Heart rate 4. Central venous pressure

Secondary

MeasureTime frame
1. Sequential Organ Failure Assessment (SOFA) score 2. Survival at 28 days 3. Length of need for catecholamine application 4. Length of need for mechanical ventilation 5. Length of need for renal replacement therapy 6. Length of stay in intensive care unit (ICU)

Countries

Austria, Germany

Outcome results

None listed

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