Skip to content

Cancelled by the investigator.A study on the effectiveness of multi-center intravenous iron drug comprehensive evaluation based on real world

A study on the effectiveness of multi-center intravenous iron drug comprehensive evaluation based on real world

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400086005
Enrollment
Unknown
Registered
2024-06-24
Start date
2024-07-01
Completion date
Unknown
Last updated
2025-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Iron deficiency anemia

Interventions

Carboxymaltose iron group:Carboxymaltose iron
Iron isomaltose group:Iron isomaltose therapy
Ferric sucrose group:Ferric sucrose therapy

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Because the sample population of this study involved multiple departments, patients in surgical departments (orthopedics, general surgery, gynecological oncology) and internal medicine departments (nephrology) had great differences in disease status, diagnosis and treatment strategy, and application needs of intravenous iron agents. Therefore, the inclusion and exclusion criteria are formulated separately: 1. General surgery, orthopedics, Gynecology (gynecologic tumor) patients: Inclusion criteria: (1) Patients undergoing elective surgery, orthopedics, gynecology (tumor) surgery; (2) Age 18 and above; (3) From January 1, 2024 to December 31, 2024, the patient was admitted to the hospital of the research Center and during the surgical treatment (perioperative period), intravenous use of percarboxyl iron maltose/iron sucrose/iron isommaltose; (4) The application indication of intravenous iron is clear and reasonable. 2. Patients in renal department: Inclusion criteria: (1) The diagnosis is consistent with the "Chinese Expert Consensus on the Diagnosis and Treatment of Renal Anemia" (2018 Revision), and there is no limit to whether hemodialysis treatment is performed; (2) Age 18 and above; (3) No history of blood transfusion in the past 3 months; (4) From January 1, 2024 to December 31, 2024, he/she was admitted to the research Center hospital and received intravenous application of percarboxyl iron maltose/iron sucrose/iron isommaltose.

Exclusion criteria

Exclusion criteria: 1. General surgery, orthopedics, Gynecology (gynecologic tumor) patients: Exclusion criteria: (1) Patients who received allogeneic blood transfusion before surgery; (2) Patients undergoing emergency surgery due to acute trauma/bone injury; (3) Currently has an infection or other major/life-threatening illness that is difficult to control; (4) Women during pregnancy; (5) Bone marrow hematopoietic dysfunction; (6) Patients with severe hyperthyroidism and hemolytic reaction; (7) Patients with incomplete clinical records or missing follow-up. 2. Patients in renal department: Exclusion criteria: (1) Combined with malignant tumor; (2) Currently has an infection or other major/life-threatening illness that is difficult to control; (3) Women during pregnancy; (4) Bone marrow hematopoietic dysfunction; (5) Patients with severe hyperthyroidism and hemolytic reaction; (6) Patients with incomplete clinical records or missing follow-up.

Design outcomes

Primary

MeasureTime frame
RBC;Hb;HCT;MCV;MCH;MCHC;

Secondary

MeasureTime frame
SF;SI;TRF;TIBC;TS;IS;Length of stay;Blood transfusion rate and volume;The interval between the onset of anemia again;

Countries

China

Contacts

Public ContactLi Zhengxiang

Tianjin Medical University General Hospital

13820893896@163.com+86 138 2089 3896

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026