ClinicalTrials.Veeva

Menu

Stability of Middle Molecule Clearance (EMIC2)

K

Klinik für Anästhesiologie

Status

Completed

Conditions

Continuous Hemodialysis

Treatments

Device: Hemodialysis with EMIC 2 filters

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01308073
EMIC2_2011_02_03

Details and patient eligibility

About

The investigators aim to show, whether all middle molecules are included in the clearance and whether this clearance is stable until 72 hours.

Full description

A better middle molecule clearance has been shown until 24 hours of duration. The investigators will extend our observations until 72 hours.

Enrollment

15 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • informed consent
  • age>18 years
  • acute renal insufficiency with indication for continuous hemodialysis, according to RILFE classification F: serum creatinine increase > 3-fold or serum creatinine > 4mg/dl with acute increase of >0,5mg/dl Urine Output <0,3mg/kg/h for 24 h or anuria for 12 h
  • body weight:60-80kg
  • anticoagulation with citrate possible and indicated
  • Dose for hemodialysis of 2l/h

Exclusion criteria

  • participation in another clinical trial within on month prior to this study

  • pregnancy or brest feeding

  • septic shock

  • interference with cystatin-C

    1. haemolysis <1g/dl
    2. Bilirubin<9mg/dl
    3. Triglyceride >700mg/dl
    4. rheumatoid factor > 300kIU/l

Trial design

15 participants in 1 patient group

EMIC 2 dialysis
Description:
Patients on ICU requiring dialysis for acute renal insufficiency
Treatment:
Device: Hemodialysis with EMIC 2 filters

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems