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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

TypeNameDescription
DIETARY_SUPPLEMENTLactoferrinLactoferrin in tablets 4g/daily
DRUGRecombinant human erythropoietinRecombinant 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.