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Efficacy and Safety of High Dose Intravenous Iron for Treatment Iron Deficiency Anemia in Gynecologic Malignancy Disease: Retrospective Cohort Study

Efficacy and Safety of High Dose Intravenous Iron for Treatment Iron Deficiency Anemia in Gynecologic Malignancy Disease: Retrospective Cohort Study

Status
Unknown
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20230815001
Enrollment
108
Registered
2023-08-15
Start date
2023-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Petient who has Iron deficiency anemia in gynecologic malignancy disease Iron deficiency anemia, iv iron, gynecologic malignancy disease

Interventions

The patient who recieved intravenous iron supplement for treatment iron deficiency anemia during chemotherapy course.,The patient who recieved standard treatment (oral iron supplement or blood transfu
Treatment,Treatment
Intervention group,Intervention group

Sponsors

Faculty of Medicine, KhonKaen university
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patient who diagnosed with gynecologic-oncology disease recieving chemotherapy between 01/01/2020-31/05/2023 in Srinagarind hospital 2. Age more than 18 years old 3. Hb < 12 g/dL 4. met criteria of inrondeficiency anemia

Exclusion criteria

Exclusion criteria: 1. Anemia due to bone marrow disease 2. Ferritin > 800 ng/ml 3. Transferring saturation equal or greater than 50% 4. Incomplete information

Design outcomes

Primary

MeasureTime frame
Blood transfusion rate at the time of complete chemotherapy course Number of blood transfusion per chemotherapy course

Secondary

MeasureTime frame
maintaing hemoglobin within 0.5 mg/dL of basline at the time of complete chemotherapy course Hemoglobin level

Countries

Thailand

Contacts

Public ContactKanynat Karasaard

Faculty of Medicine, KhonKaen University

Kanyka@kkumail.com0850116612

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026