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Iatrogenic Deficiencies in ICU Patients With Prolonged Continuous Renal Replacement Therapy

Iatrogena bristtillstånd Hos intensivvårdade Patienter Under långvarig Behandling Med Kontinuerlig Dialys

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06983197
Acronym
IBRIST
Enrollment
30
Registered
2025-05-21
Start date
2025-06-01
Completion date
2029-12-31
Last updated
2025-05-21

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

Conditions

Acute Kidney Injury

Brief summary

ICU patients are recruited after at least 5 days treatment with continuous renal replacement therapy. Blood samples are drawn at time of recruitment and then every 3-5 days until ceseation of renal replacement therapy. Samples will be analyzed for concentrations of trace elements, vitamins and amino acids. 10 adult ICU patients treated for two weeks without renal replacement therapy will be sampled at one time point to serve as controls.

Interventions

DIAGNOSTIC_TESTblood test

Blood samples are drawn every 3-5 days in the RRT group but only once in the control group

Sponsors

Karolinska University Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

CRRT group: * CRRT more than 5 days

Exclusion criteria

* N/A Inclusion criteria non-CRRT group \- ICU care 10-15 days without any dialysis treatment

Design outcomes

Primary

MeasureTime frameDescription
Concentration of trace elementFrom enrollment to the end of treatment at 4 weeksMeasurments of trace elements and vitamins as compared to established reference values as well as non-CRRT controls

Secondary

MeasureTime frameDescription
Amino acidsFrom enrollment to the end of treatment at 4 weeksConcentration of amino acids in plasma
VitaminsAt all measuring pointsWater soluble vitamins, concentration in plasma. Compared to non-crrt controls and established references

Contacts

Primary ContactJonathan Grip, MD, PhD
jonathan.grip@regionstockholm.se+46 73 623 09 06
Backup ContactKristina Kilsand, Research nurse
kristina.kilsand@regionstockholm.se+46 8 123 810 03

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026