The Effect of Preoperative Intravenous Ferric Derisomaltose and EPO and Tranexamic Acid in Patients With Preoperative Anemia or Iron Deficiency in Bone Tumor
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: isomaltose iron.
- Who it may be relevant to
- Registry conditions: Anemia. Basic parameters: 18 years — 65 years · 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 →
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Official title
The Effect of Preoperative Intravenous Ferric Derisomaltose and EPO and Tranexamic Acid Versus Usual Treatment in Patients With Preoperative Anemia or Iron Deficiency in Bone Tumor: a Single-center, Prospective, Open-label, RCT Study
Overview
The pelvis and spine are common sites of primary and secondary bone tumors, and most patients require surgical treatment. However, due to bleeding, high tumor burden, and other reasons, iron deficiency anemia (IDA) is common in these patients. At present, allogeneic blood resources are scarce in China and even globally, and cancer patients cannot undergo autologous blood transfusion. In addition, there is a large amount of bleeding during pelvic and spinal open surgery, which collectively leads to a high incidence of perioperative anemia in patients with pelvic and spinal tumors, and even the loss of surgical opportunities. Therefore, perioperative blood management for bone tumor surgery is extremely important. The combination of intravenous iron and EPO has been proven to rapidly improve the hemoglobin levels of perioperative surgical patients in previous studies, but there is currently no research related to bone tumors. This study uses a single center, prospective, open label, randomized controlled clinical trial to explore the effects of preoperative application of intravenous isomaltose iron combined with erythropoietin and tranexamic acid compared to conventional treatment in patients with preoperative anemia or iron deficiency in bone tumor surgery, hoping to establish a standard paradigm for perioperative blood management in bone tumor patients.
Interventions
- Drug isomaltose iron
Calculate the patient's iron requirement based on a simplified scale for the isomaltose iron group; Yibiao 150IU/kg subcutaneous injection, no treatment in the conventional treatment group; 0.5g of tranexamic acid is administered locally after dilution before surgical closure
Primary outcome measures
- Hb levels 21 days after surgery [Time frame: Day 21]
Secondary outcome measures (2)
- Blood transfusion rate within 21 days after surgery [Time frame: Day 21]
- Hb levels 14 days after surgery [Time frame: Day 14]
Eligibility criteria
Inclusion criteria
- Patients aged 18 and above with primary malignant bone tumors and bone metastases who plan to undergo open surgery for the sacrum, pelvis, and spine.
- 5 ± 2 days before surgery, hemoglobin<130g/L, or iron deficiency (TSAT<20%)
- Patients are able to understand the research content and sign informed consent forms
Exclusion criteria
Meet any of the following criteria;
- Ferritin>800 ng/ml or hemoglobin<70 g/L
- Expected survival period less than six months
- Women who are pregnant, breastfeeding, or planning to conceive
- Known to have allergic reactions to other iron agents
- Severe bone marrow suppression event (4th degree bone marrow suppression) occurred 4 weeks before enrollment
- Decompensated stage of liver disease
- Patients with combined acute phase infections
- Chronic kidney disease stage 3-5
- Patients who received oral iron, intravenous iron, EPO, or blood transfusion treatment within one month prior to the start of the study.
- Researchers believe that other conditions that are not suitable for participation in this study, such as deafness, Parkinson's disease, communication disorders, etc
- Participated in other clinical trials within the three months prior to participating in this study
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07314424 · PKUPH-anemia-001