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Nutritional Regulation of Leukocyte Function (FPP Supplement)

Primary Purpose

FPP, Fermented Papaya Preparation, Supplements

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
FPP supplement
Sponsored by
Indiana University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for FPP focused on measuring fermented papaya, wound healing responses

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Ages 18 and above
  • Subjects must be able to follow directions and give informed consent on their own

Exclusion Criteria:

  • • Individuals who are deemed unable to understand the procedures, risks and benefits of the study, ie. Informed consent will be excluded.

    • Females who are pregnant will also be excluded to minimize the risk to such individuals (and fetus).
    • Individuals who are therapeutically immuno-compromised will also be excluded to decrease statistical variability and to minimize potential of confounders.
    • Candidates for inclusion into the study will not include individuals as defined in 45 CFR 46 Subparts B, C and D, nor from any other population which may be considered vulnerable.

Sites / Locations

  • Indiana University Health Methodist Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

No Intervention

Experimental

Experimental

Experimental

Arm Label

control

3 grams of supplements

6 grams of supplements

9 grams of supplements

Arm Description

no supplements will be taken

subjects will take 3 grams of supplements once per day

subjects will take 3 grams of supplements twice per day

subjects will take 3 grams of supplements three times per day

Outcomes

Primary Outcome Measures

Reactive Oxygen species (ROS) production of Leucocytes 6 weeks post supplementation
The major objectives of the study is to study the mechanism of action on ROS production by leucocytes of healthy subjects post 6 weeks FPP supplementation measured by flowcytometry
Blood leukocyte phagocytosis 6 weeks post supplementation
Blood leukocyte phagocytosis 6 weeks post supplementation via cell biology technique

Secondary Outcome Measures

Leukocyte activation and cytokine production at 6 wks post supplementation
Blood leukocyte activation and cytokine production at 6 weeks post supplementation will be measured via flow cytometry

Full Information

First Posted
December 2, 2021
Last Updated
August 17, 2023
Sponsor
Indiana University
Collaborators
Osato Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT05191758
Brief Title
Nutritional Regulation of Leukocyte Function
Acronym
FPP Supplement
Official Title
Nutritional Regulation of Leukocyte Function
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
February 15, 2022 (Actual)
Primary Completion Date
July 8, 2022 (Actual)
Study Completion Date
July 31, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indiana University
Collaborators
Osato Research Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of the current study is to determine the dose at which Fermented Papaya Preparation ( FPP) is able to improve inducible respiratory burst outcomes in peripheral blood mononuclear cells (PBMC) and neutrophils of participants. Our investigators have reported that supplementation with standardized fermented papaya preparation (FPP) in mice improves dermal wound healing outcomes. Therefore, based on these observations, the investigators propose to study the dose at which FPP supplementation induces respiratory burst in blood-derived myeloid cells in healthy subjects.
Detailed Description
Fermented Papaya Preparation (FPP) is a dietary supplement that is available as over-the-counter in the US. FPP possesses antioxidant properties, which provide benefit against age-related complications[]. Chronic wounds in patients with diabetes represent a major public health problem. Previous studies from the investigators have demonstrated that wound-site macrophages from patients with diabetes are compromised in their ability to support wound healing. Several independent observations convergently point toward the hypothesis that treatment with papaya preparations may facilitate wound healing responses. Our laboratory reported the first evidence demonstrating that FPP may improve diabetic wound outcomes by specifically influencing the response of wound-site macrophages and the subsequent angiogenic response. FPP has a long track record of safe human consumption. The objective of the current study is to determine the dose at which FPP is able to improve inducible respiratory burst outcomes in peripheral blood mononuclear cells (PBMC) and neutrophils of participants. Our investigators have reported that supplementation with standardized fermented papaya preparation (FPP) in mice improves dermal wound healing outcomes. Therefore, based on these observations, the investigators propose to study the dose at which FPP supplementation induces respiratory burst in blood-derived myeloid cells in healthy subjects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
FPP, Fermented Papaya Preparation, Supplements, Diabetic Wound, Healing Wound
Keywords
fermented papaya, wound healing responses

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
31 (Actual)

8. Arms, Groups, and Interventions

Arm Title
control
Arm Type
No Intervention
Arm Description
no supplements will be taken
Arm Title
3 grams of supplements
Arm Type
Experimental
Arm Description
subjects will take 3 grams of supplements once per day
Arm Title
6 grams of supplements
Arm Type
Experimental
Arm Description
subjects will take 3 grams of supplements twice per day
Arm Title
9 grams of supplements
Arm Type
Experimental
Arm Description
subjects will take 3 grams of supplements three times per day
Intervention Type
Dietary Supplement
Intervention Name(s)
FPP supplement
Other Intervention Name(s)
Fermented Papaya Preparation Supplement (FPP), FPP
Intervention Description
Participants will take the supplements per randomization
Primary Outcome Measure Information:
Title
Reactive Oxygen species (ROS) production of Leucocytes 6 weeks post supplementation
Description
The major objectives of the study is to study the mechanism of action on ROS production by leucocytes of healthy subjects post 6 weeks FPP supplementation measured by flowcytometry
Time Frame
6 weeks post supplementation
Title
Blood leukocyte phagocytosis 6 weeks post supplementation
Description
Blood leukocyte phagocytosis 6 weeks post supplementation via cell biology technique
Time Frame
6 weeks post supplementation
Secondary Outcome Measure Information:
Title
Leukocyte activation and cytokine production at 6 wks post supplementation
Description
Blood leukocyte activation and cytokine production at 6 weeks post supplementation will be measured via flow cytometry
Time Frame
5 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Ages 18 and above Subjects must be able to follow directions and give informed consent on their own Exclusion Criteria: • Individuals who are deemed unable to understand the procedures, risks and benefits of the study, ie. Informed consent will be excluded. Females who are pregnant will also be excluded to minimize the risk to such individuals (and fetus). Individuals who are therapeutically immuno-compromised will also be excluded to decrease statistical variability and to minimize potential of confounders. Candidates for inclusion into the study will not include individuals as defined in 45 CFR 46 Subparts B, C and D, nor from any other population which may be considered vulnerable.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sashwati Roy, PhD
Organizational Affiliation
Indiana University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Indiana University Health Methodist Hospital
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46228
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Nutritional Regulation of Leukocyte Function

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