The Effectiveness of Lactoferrin in the Management of Treatment-induced Anemia
NCT03683810 · Status: UNKNOWN · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 50
Last updated 2022-09-06
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.
Conditions
Interventions
- DIETARY_SUPPLEMENT
-
Lactoferrin
Lactoferrin in tablets 4g/daily
- DRUG
-
Recombinant human erythropoietin
Recombinant human erythropoietin (rHuEPO, epoetin alfa)
Sponsors & Collaborators
-
Hematological Clinic - Nicosia General Hospital
collaborator UNKNOWN -
German Oncology Center, Cyprus
collaborator OTHER -
Limassol Hematology-oncology Center
collaborator UNKNOWN -
Cyprus University of Technology
lead OTHER
Principal Investigators
-
Andreas CHARALAMBOUS · Cyprus University of Technology (Nursing Department)
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-01-14
- Primary Completion
- 2023-01-31
- Completion
- 2023-06-30
Countries
- Cyprus
Study Locations
More Related Trials
-
Lactoferrin Versus Ferrous Sulfate in Iron-deficiency During Pregnancy
NCT03759353 ·Status: COMPLETED ·Phase: PHASE2
-
Effects of 5-Aminolevulinic Acid on Iron Deficiency Anemia
NCT01380548 ·Status: COMPLETED ·Phase: NA
-
Lactoferrin Versus Ferrous Fumarate for Treatment of Mild to Moderate Iron Deficiency Anemia During Pregnancy
NCT03484845 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
Ferrous Sulphate Supplement (V0355) in Women With Iron Deficiency Anaemia
NCT02518568 ·Status: TERMINATED ·Phase: PHASE1
-
Iron Balance Study of DFO and GT56-252 in Patients With Transfusional Iron Overload Secondary to Beta-Thalassemia
NCT00069862 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Bovine Lactoferrin to Prevent and Cure Iron Deficiency and Iron Deficiency Anemia in Complicated Pregnancies
NCT01221844 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety of Oral Deferasirox (20 mg/kg/d) in Pts 3 to 6 Months After Allogeneic Hematopoietic Cell Transplantation Who Present With Iron Overload
NCT00654589 ·Status: COMPLETED ·Phase: PHASE4
-
An Extension Study of Iron Chelation Therapy With Deferasirox (ICL670) in β-thalassemia Patients With Transfusional Iron Overload
NCT00171210 ·Status: COMPLETED ·Phase: PHASE3
-
Open-Label Study of Oral CEP-701 (Lestaurtinib) in Patients With Polycythemia Vera or Essential Thrombocytosis
NCT00586651 ·Status: COMPLETED ·Phase: PHASE2
-
A Trial Comparing Ferumoxytol With Placebo for the Treatment of Iron Deficiency Anemia
NCT01114139 ·Status: COMPLETED ·Phase: PHASE3
-
Evaluate the PK, Safety, Tolerability of Ferric Maltol at 3 Dosage Levels in Paediatric Subjects With Iron Deficiency
NCT03181451 ·Status: COMPLETED ·Phase: PHASE1
-
Four-Way Crossover Study to Compare Ferric Maltol Capsules and Oral Suspension in Healthy Volunteers
NCT04626414 ·Status: COMPLETED ·Phase: PHASE1
-
Impact of Preoperative Treatment of Anemia and Iron Deficiency in Cardiac Surgery on Outcome.
NCT02031289 ·Status: COMPLETED ·Phase: PHASE4
-
Low-dose Iron Supplementation and Markers of Iron Status Among Non-anemic, Iron-deficient Women
NCT02683369 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Trial Protocol GlobiFer - Oral Iron Repletion
NCT03055559 ·Status: COMPLETED
-
A Study Comparing the Iron Substitution With the Medicinal Products Ferinject or Monofer
NCT02905539 ·Status: COMPLETED ·Phase: PHASE4
-
Effect of Iron Status on Occurrence of Non-transferrin-bound Iron (NTBI) in Serum in Response to an Oral Iron Load
NCT02831712 ·Status: UNKNOWN ·Phase: NA
-
Pharmacokinetics, Pharmacodynamics and Safety of Epeleuton in Patients With Sickle Cell Disease
NCT05861453 ·Status: COMPLETED ·Phase: PHASE2
-
Improvement of Fatigue Symptoms in the Iron Deficiency Anemia With Iron Succinylate Therapy
NCT03873584 ·Status: WITHDRAWN
-
Total Dose Infusion of Ferumoxytol(1020mg) in 15 Minutes for Iron Deficiency Anemia
NCT01374919 ·Status: COMPLETED ·Phase: NA
-
Intravenous Iron in Adults With Cystic Fibrosis
NCT03632525 ·Status: COMPLETED ·Phase: PHASE4
-
Different Iron Supplements for Prevention of Anemia in Pregnancy
NCT02487719 ·Status: UNKNOWN ·Phase: PHASE4
-
Assess the Feasibility and Safety of Granulocyte Colony Stimulating Factor (GCSF) Mobilization of CD34+ Hematopoietic Progenitor Cells in Patients With Betathalassemia Major
NCT00658385 ·Status: COMPLETED ·Phase: NA
-
Effectiveness of Low-dose Iron Treatment in Non-anaemic Iron-deficient Women
NCT04636060 ·Status: COMPLETED ·Phase: NA
-
Identification of Mechanism in the Erythroid Response in Patients With Myelodysplasia Undergoing Chelation Therapy
NCT01956799 ·Status: COMPLETED