The Effect of Fermented Papaya Preparation on Patients With Chronic Kidney Disease Under Dialysis Receiving Intravenous Iron
Primary Purpose
Anemia, Chronic Kidney Disease Stage 5
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
fermented papaya preparation
Sponsored by
About this trial
This is an interventional treatment trial for Anemia
Eligibility Criteria
Inclusion Criteria:
- Age 18-70. Any primary kidney disease resulting in ESRD. Hemodynamically stable status. PTH up to 2-9 times upper normal limits. Patients receiving ESA may be included.
Exclusion Criteria:
- Any evidence of acute bleeding. Hg level of less than 8 g/dL Patients with known allergy to Papaya
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
FPP arm
Arm Description
active treatment with fermented papaya preparation
Outcomes
Primary Outcome Measures
Iron status
evaluation of iron overload reduction after 3 months of treatment with fermented papaya preparation
Secondary Outcome Measures
Full Information
NCT ID
NCT03005847
First Posted
December 26, 2016
Last Updated
January 18, 2017
Sponsor
Hadassah Medical Organization
1. Study Identification
Unique Protocol Identification Number
NCT03005847
Brief Title
The Effect of Fermented Papaya Preparation on Patients With Chronic Kidney Disease Under Dialysis Receiving Intravenous Iron
Official Title
The Effect of Fermented Papaya Preparation on Patients With Chronic Kidney Disease Under Dialysis Receiving Intravenous Iron
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Unknown status
Study Start Date
March 2017 (undefined)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hadassah Medical Organization
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Fermented papaya preparation has been reported to bind and neutralize reactive oxygen species as well as iron. Patients undergoing hemodialysis are generally on iron overload status due to their inability to use iron storage adequately. The aim of this study is to evaluate the effect of FPP on the iron status of these patients.
Detailed Description
Background and rationale
Patients with chronic kidney disease (CKD) on hemodialysis often suffer from anemia. The anemia is primarily caused by insufficient production by the failing kidneys of the erythroid stimulating hormone - erythropoietin (Epo). Oxidative stress may be another reason for anemia. Oxidative stress in RBCs of these patients may be caused by:
Passage of the blood through the plastic tubing during the dialysis procedure. We have shown oxidative stress in RBCs following passage of blood through similar tubing during leukopheresis procedure (1). Other groups reported similar effects during hemodialysis.
Iron overload - In order to maximize the effect of Epo, the treatment is supplemented by IV injection of iron. This iron may accumulate and cause iron overload in some hemodialyzed patients. Under normal conditions, iron is transported in the blood and enters into cells following binding the plasma protein transferrin. However, when iron content in the plasma exceeds the binding capacity of transferrin, non-transferrin-bound iron (NTBI) appears. This iron enters cells via alternative pathways, and accumulates in the cytosol, where it participates in chemical reactions (Haber-Weiss, Fenton) that generate reactive oxygen species (ROS). Excess ROS overcomes the protective cellular anti-oxidant mechanisms and becomes cytotoxic. In the erythroid system, excess ROS causes accelerated apoptosis (programmed cell death) of precursor cells in the bone marrow and a short survival of mature RBCs in the circulation, resulting in chronic anemia. Excess iron and ROS may also damage other cells and lead to malfunctioning of vital organs, such as the heart and liver (2,3).
FPP has been reported to bind and neutralize (scavenge) ROS (4) as well as free iron (chelate) (5). Both activities ameliorate the oxidative stress.
Treatment with FPP of various diseases associated with oxidative stress, administered orally (3 gr. X 3 times a day), have been shown to significantly ameliorate the symptoms underlying these diseases (6-18). FPP has a long track-record of safe human consumption (19-20). It has been used for many years as a food-supplement by thousands of people around the world without any reported side effect.
Research goals
To study the effect of fermented papaya preparation (FPP) on patients with chronic kidney disease (CKD) under dialysis, receiving intravenous iron.
General Protocol:
This will be a single-arm, open-label, single-center study in 20 patients upon dialysis receiving IV iron supplementation. All participants will be treated with FPP for 3 months.
Bi-weekly, blood samples will be drawn and the patients will be monitored for assessment of safety and efficacy.
Detailed Protocol Twenty patients, treated on Hadassah Medical center, Jerusalem, will be screened and recruited according to clinical criteria.
inclusion criteria: Age 18-70. Any primary kidney disease resulting in ESRD. Hemodynamically stable status. PTH up to 2-9 times upper normal limits. Patients receiving ESA may be included.
Exclusion criteria:
Any evidence of acute bleeding. Hg level of less than 8 g/dL Patients with known allergy to Papaya
3. Patients will be treated orally with FPP (3 gr. X 3 times a day) for 3 months.
4. Blood samples will be obtained from all patients prior and during (every 2 weeks) treatment.
5. Samples will be analyzed for:
Blood chemistry for Potassium, Albumin and Phosphorous (every 2 weeks).
Anemia: Complete blood count, including RBC number and indexes, as well as hemoglobin content.
Oxidative stress: (once monthly) Reactive oxygen species Reduced glutathione Membrane lipid peroxidation External phosphatidylserine
Iron overload: (once monthly) Serum ferritin Serum transferin. Labile plasma iron Serum hepcidin Intracellular labile iron pool
Safety measures:
Adverse events: Frequency, severity, seriousness, time to onset, duration, and relatedness to study product.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anemia, Chronic Kidney Disease Stage 5
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
FPP arm
Arm Type
Experimental
Arm Description
active treatment with fermented papaya preparation
Intervention Type
Dietary Supplement
Intervention Name(s)
fermented papaya preparation
Other Intervention Name(s)
FPP
Intervention Description
dietary supplementation with fermented papaya preparation
Primary Outcome Measure Information:
Title
Iron status
Description
evaluation of iron overload reduction after 3 months of treatment with fermented papaya preparation
Time Frame
3 months of treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 18-70. Any primary kidney disease resulting in ESRD. Hemodynamically stable status. PTH up to 2-9 times upper normal limits. Patients receiving ESA may be included.
Exclusion Criteria:
Any evidence of acute bleeding. Hg level of less than 8 g/dL Patients with known allergy to Papaya
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Itamar Sagiv, MD
Phone
97226776881
Email
itamar@hadassah.org.il
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
itamar sagiv, MD
Organizational Affiliation
Hadassah Medical Organization
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
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The Effect of Fermented Papaya Preparation on Patients With Chronic Kidney Disease Under Dialysis Receiving Intravenous Iron
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