RecruitingPhase 3NCT05744219

Improved Recovery by Iron Following Surgery With Blood Loss, the IRIS-trial

Improved Recovery by Iron Following Surgery With Blood Loss, a Double-blind Multi-centre Randomized Controlled Phase III Drug Trial (the IRIS-trial)


Sponsor

Jon Unosson

Enrollment

338 participants

Start Date

Sep 4, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The aim of the study is to investigate if iv iron formulation improve recovery after surgery with blood loss. Post-operative anaemia is a common debilitating condition after major surgery due to a combination of preoperative iron deficiency anaemia (IDA) and per-operative blood loss. Median blood loss following hepatopancreatobiliary (HPB) and complex aortic surgery typically range between 500-1000 ml. Bioavailability of iron may be a rate limiting factor in erythropoiesis in anaemia secondary to blood loss. For the IRIS trial, it is hypothesized that intravenously (iv) administered Ferric Carboxymaltose after a per-operative blood loss of 400-4000 ml, improves post-operative recovery and reduces the RBC transfusion. Patients scheduled for elective HPB surgery or complex aortic surgery will be screened for eligibility and recruited into the study. By the end of the surgical procedure, if blood loss is estimated to 400-4000 ml, the patient is randomized 1:1 to iv 1000 mg Ferric Carboxymaltose or placebo. The primary endpoint is a composite of death, number of RBC transfusions, post-operative severe anemia (Hb \<80 g/L) and FACT-An Quality of life (QoL) five weeks after surgery, assessed by win ratio. The trial will also examine effects on; a) levels of Hb; b) markers of erythropoiesis and iron bioavailability; c) post-operative complications; d) post-operative recovery; e) performance status; f) subgroups based on type of surgery and degree of anemia and iron deficiency; g) re-admissions; h) long term outcome based on patient medical records and i) how post-operative recovery differs between those with low (\<400 ml), high (400-4000 ml) and very high (\>4000 ml) per-operative blood loss. Recruitment will continue until 338 patients are randomized or 304 have completed the five week follow up The coordinating center of the trial is the Department of Surgery at Uppsala University Hospital. Participating sites are also Linköping University Hospital and Lund University Hospital, all in Sweden. Other sites may be added.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study (called the IRIS trial) is testing whether giving intravenous iron after major surgery involving significant blood loss — such as complex aortic surgery, liver removal, or pancreatic surgery — can speed up recovery and reduce anemia (low red blood cell counts) compared to standard care. **You may be eligible if...** - You are over 18 years old - You weigh more than 50 kg - You are scheduled for complex aortic surgery, liver resection (partial removal), or pancreatic resection - You are able to provide written consent **You may NOT be eligible if...** - Your expected survival is less than 6 months - You received intravenous iron therapy within the past month - You have severe anemia before surgery - You have a condition that causes iron overload (such as hemochromatosis) - You are on dialysis before surgery - You are enrolled in another drug or device study within 30 days - You have another major surgery planned within 5 weeks - You are pregnant Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGFerric carboxymaltose

Active drug

DRUGPlacebo

Placebo


Locations(1)

Uppsala University Hospital

Uppsala, Sverige, Sweden

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NCT05744219


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