Clinical trial

Intravenous Ferric Carboxymaltose Versus Oral Ferrous Sulfate Replacement in Anaemia Due to Acute Nonvariceal Gastrointestinal Bleeding (FIERCE): Protocol of a Multicentre Randomised Controlled Trial

Name
46395-5/2021/EÜIG
Description
Anemia is a frequent complication of gastrointestinal bleeding, affecting 61% of the patients. Currently, anemia caused by gastrointestinal bleeding can be treated with iron supplementation. However, the dose and route of the administration are still a question. The FIERCE clinical trial aims to compare the effect of intravenous iron supplementation and oral iron replacement on mortality, unplanned emergency visits, and hospital readmissions in multimorbid patients with acute nonvariceal gastrointestinal bleeding.
Trial arms
Trial start
2024-09-01
Estimated PCD
2026-12-31
Trial end
2027-02-01
Status
Not yet recruiting
Phase
Early phase I
Treatment
Oral iron supplementation
Ca. 200-300 mg of ferrous sulfate will be administered orally every day for 3 months.
Arms:
Oral iron supplementation
Intravenous iron supplementation
One dose of intravenous 1000 mg ferric carboxymaltose will be administered on the day of randomization.
Arms:
Intravenous iron supplementation
Size
570
Primary endpoint
Composite outcome
3 months
Eligibility criteria
Inclusion Criteria: 1. age ≥ 65 years; 2. endoscopically proven acute nonvariceal GIB source; 3. 48 hours after the endoscopic diagnosis and/or treatment; 4. hemodynamically stable; 5. the discharge of the patient is planned; 6. hemoglobin level \<10 g/dl on the day of randomisation; 7. 24 hours after the last transfusion and no need for further transfusion; 8. signed informed consent. Exclusion Criteria: 1. known hypersensitivity to iron products (mild side effects excluded); 2. previous diagnosis of iron overload \[e.g., transferrin receptor saturation (TSAT) \>50%, ferritin\> 160 for women ng/ml, ferritin \>270 ng/ml for men) or disorders of iron utilisation; 3. pregnancy or breast feeding; 4. diagnosis of iron malabsorption (at discretion of the attending clinician; e.g., severe inflammatory bowel disease, active celiac disease); 5. chronic end stage diseases (chronic heart failure-New York Heart Association Classification class 4, chronic kidney disease (eGFR \<30 mL/min/1.73 m2) with or without dialysis, liver cirrhosis with Child Pugh C score, chronic kidney disease with dialysis, chronic obstructive pulmonary disease stage 4, chronic inflammatory disease, malignancies, AIDS); 6. active malignancies; 7. liver cirrhosis with known varices at high risk of bleeding - endoscopic features of high risk of variceal bleeding or liver stiffness measured by transient elastography \>20 kiloPascal and platelet count \<150 × 10\^9 cells/L; 8. gastrointestinal tract malignancies with high risk of gastrointestinal bleeding; 9. high risk of poor compliance or no fixed abode; 10. myelo- or lymphoproliferative diseases; 11. anemia not attributable to iron deficiency (sideroblastic anaemia, aplastic anaemia, haemolytic anaemia, thalassaemia, B12 vitamin or folic acid deficiency or combination of these with IDA); 12. primary coagulation disorders (e.g. Glanzmann thrombasthenia, Von Willebrand disease, Haemophylia A, Haemophylia B); 13. the patient will be transferred to another institute after discharge (e.g. hospital, senior care center); 14. Eastern Cooperative Oncology Group (ECOG) Performance Status \>2.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'The investigators plan to recruit 285 patients on each arm.', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 570, 'type': 'ESTIMATED'}}
Updated at
2023-11-28

1 organization

2 products

2 indications

Organization
University of Pecs
Indication
Anaemia