Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
24 participants
OBSERVATIONAL
2012-05-31
2015-02-19
Brief Summary
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Detailed Description
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The objective of the current study is to determine whether FPP is able to improve inducible respiratory burst outcomes in peripheral blood mononuclear cells (PBMC) of participants with diabetes. Our investigators have recently reported that supplementation with standardized fermented papaya preparation (FPP) in adult diabetic mice improves dermal wound healing outcomes. The production of reactive oxygen species (ROS) by type 2 diabetics (T2DM) PBMC is markedly inhibited compared to that of the PBMC from non-diabetic donors. We observed that ex vivo FPP supplementation corrected such inhibition in ROS production by PBMC from T2DM donors. Therefore, based on these observations, the investigators propose to study the outcome that FPP supplementation has in patients with diabetes.
Conditions
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Study Design
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OTHER
OTHER
Study Groups
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Fermented Papaya Preparation (FPP)
This a is single arm study - all participants will receive and take fermented papaya preparation (FPP) for a total of 6 weeks. Participants will take 3 grams of FPP three times per day (a total of 9 grams per day).
Fermented Papaya Preparation (FPP)
Participants will take fermented papaya preparation (FPP) for a total of 6 weeks (3 grams, three times each day for a total of 9 grams per day). The participants will attend 5 study visits and have their blood draw at each visit (5 total times).
Interventions
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Fermented Papaya Preparation (FPP)
Participants will take fermented papaya preparation (FPP) for a total of 6 weeks (3 grams, three times each day for a total of 9 grams per day). The participants will attend 5 study visits and have their blood draw at each visit (5 total times).
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Diabetic subjects selected for the study will meet one or more of the following criteria as recommended by American Diabetes Association:
* 1\) Symptoms of diabetes and casual plasma glucose 200 mg/dl (11.1 mmol/l) (casual is defined as any time of day without regard to time since last meal. The classic symptoms of diabetes include polyuria, polydipsia, and unexplained weight loss); OR
* 2\) Fasting plasma glucose (FPG) 126 mg/dl (7.0 mmol/l) (fasting is defined as no caloric intake for at least 8 h); OR
* 3\) 2-hr plasma glucose 200 mg/dl (11.1 mmol/l) during an oral glucose tolerance test (OGTT) (this test should be performed as described by the World Health Organization, using a glucose load containing the equivalent of 75g anhydrous glucose dissolved in water)
Exclusion Criteria
* T2DM with HbA1c = 9.1 or above
* BMI less than 22 and over 42
* Clinically significant kidney or liver disease
* Severe neurologic dysfunction
* Females who are pregnant as well as individuals who are therapeutically immuno-compromised will also be excluded in order to minimize the risk to such individuals (and fetus) and to decrease statistical variability and to minimize the 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
* Pregnant women are excluded to minimize the risk to such individuals (and fetus) and to decrease statistical variability and to minimize the potential of confounders
30 Years
80 Years
ALL
No
Sponsors
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Osato Research Institute
OTHER
Ohio State University
OTHER
Responsible Party
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Principal Investigators
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Sashwati Roy, PhD.
Role: PRINCIPAL_INVESTIGATOR
Ohio State University
Locations
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OSU CarePoint East
Columbus, Ohio, United States
University Hospital East (Wound Center)
Columbus, Ohio, United States
University Hospital East, OSUWMC Diabetes Clinic
Columbus, Ohio, United States
The Ohio State University/Ohio State University Wexner Medical Center
Columbus, Ohio, United States
OSUWMC Comprehensive Wound Care Center, Martha Morehouse Medical Plaza
Columbus, Ohio, United States
Countries
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Other Identifiers
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20120293
Identifier Type: -
Identifier Source: org_study_id
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