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Not yet recruiting NCT06983197

Iatrogenic Deficiencies in ICU Patients With Prolonged Continuous Renal Replacement Therapy

— Observational Acute Kidney Injury

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: blood test.
Who it may be relevant to
Registry conditions: Acute Kidney Injury. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Iatrogena bristtillstånd Hos intensivvårdade Patienter Under långvarig Behandling Med Kontinuerlig Dialys

Overview

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

Primary outcome measures

  • Concentration of trace element [Time frame: From enrollment to the end of treatment at 4 weeks]
Secondary outcome measures (2)
  • Amino acids [Time frame: From enrollment to the end of treatment at 4 weeks]
  • Vitamins [Time frame: At all measuring points]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06983197 · 2024-07642-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗