Trials / Unknown
UnknownNCT03683810
The Effectiveness of Lactoferrin in the Management of Treatment-induced Anemia
The Effectiveness of Lactoferrin in the Management of Treatment-induced Anemia in Hematological Patients
- Status
- Unknown
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- Cyprus University of Technology · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This will be a randomised control trial designed to test the effectiveness of lactoferrin in the management of treatment-induced anemia in patients with hematological malignancies.
Detailed description
Chemotherapy induced anemia (CIA) is a common adverse event in cancer patients reported to occur in 20-60% whilst the resulting low hemoglobin level is associated with impaired quality of life. Lactoferrin (LF) is a non-haem iron-binding protein that is part of the transferrin protein family, along with serum transferrin, ovotransferrin, melanotransferrin and the inhibitor of carbonic anhydrase, whose function is to transport iron in blood serum. The aim of the study is to test the effectiveness of LF along with standard care in the management of treatment-induced anemia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Lactoferrin | Lactoferrin in tablets 4g/daily |
| DRUG | Recombinant human erythropoietin | Recombinant human erythropoietin (rHuEPO, epoetin alfa) |
Timeline
- Start date
- 2019-01-14
- Primary completion
- 2023-01-01
- Completion
- 2023-06-01
- First posted
- 2018-09-25
- Last updated
- 2022-09-06
Locations
2 sites across 1 country: Cyprus
Source: ClinicalTrials.gov record NCT03683810. Inclusion in this directory is not an endorsement.