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Anemia of Inflammation and Deficiency Anemia (AIDA)

I

Iuliu Hatieganu University of Medicine and Pharmacy

Status

Unknown

Conditions

Anemia of Chronic Disease
Anemia, Iron Deficiency

Study type

Observational

Funder types

Other

Identifiers

NCT04071067
89/8.04.2019

Details and patient eligibility

About

Critical patients which requiring admission to intensive care (IT) are a special group of patients. In these patients the prevalence of anemia reported in studies is 75%. This prevalence is similar to that in the retrospective observational study conducted in our intensive care unit(ICU). Of the 783 patients included in the study, 551 (73.37%) had anemia on admission. Frequently anemia is present on discharge from ICU or hospital and may persist for an average of 11 weeks. Some studies have reported the presence of anemia as far as 6 months after discharge. It is widely accepted that anemia has a negative impact on rehabilitation and quality of life, but the treatment can not be exclusively based on blood products due to the risks associated with transfusion. Alternative treatments such as injectable iron or erythropoietin should be considered.

The Transfusion Management Initiative Group recently issued recommendations on perioperative anemia. Similar recommendations for ICU have not yet been developed in Romania. The current study has two main purposes. The first to adopt the perioperative anemia diagnostic algorithm and adapt it to anemic patients on ICU; the second to identify patients with mixed anemia (inflammatory and iron deficient anemia) who can benefit from treatment with iron.

Enrollment

1,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients admitted to ICU

ICU stay >48hours

Exclusion criteria

  • Refusal to participate in the study
  • Allergy to iron products
  • Anemia requiring massive transfusion in the last 7 days
  • Treatment of iron products in the last 7 days
  • Chronic renal failure with GFR <30mL / min or on dialysis
  • Metabolism of iron
  • Pregnant or lactation patients
  • Rheumatic diseases
  • Inflammatory bowel diseases
  • Hematological pathologies
  • Impossibility of performing laboratory tests within 72 hours of admission

Trial design

1,000 participants in 2 patient groups

Emergency Clinical County Hospital Group
Municipal Clinical Hospital Group

Trial contacts and locations

2

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Central trial contact

Robert Szabo, Resident MD

Data sourced from clinicaltrials.gov

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