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Modulating Effects of Oil Palm Phenolics in Subjects With Pre-diabetes (PREDOPP)

Primary Purpose

Prediabetes

Status
Withdrawn
Phase
Phase 1
Locations
Malaysia
Study Type
Interventional
Intervention
Oil Palm Phenolics
Placebo
Sponsored by
Universiti Sains Malaysia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prediabetes

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Subject with "pre-diabetes", i.e. fasting plasma glucose level of more than 5.6 mmol/L and less than 7.0 mmol/L; or 2-hr plasma glucose load level of more than 7.8 mmol/L and less than 11.0 mmol/L.
  • Subjects or his/her legally acceptable representative is willing to provide written informed consent.

Exclusion Criteria:

  • Subject with terminal cancer.
  • Subject with renal failure (serum creatinine more than 200 umol/L).
  • Subject with significant liver impairment (liver function test of 5 times more than the upper limit level).
  • Subject with severe dementia and psychosis.
  • Subject requires of long term corticosteroid treatment for the underlying disease such as connective tissue disorder.
  • Subject with hemoglobinopathy or anemia.
  • Subject underwent splenectomy or suffered from splenomegaly.
  • Subject with pre-existing cardiovascular disease.
  • Subject with chronic substance abuse such as chronic alcoholism or chronic opiate usage.
  • Female subject of childbearing potential unless subject underwent bilateral tubal ligation, bilateral oophorectomy or hysterectomy previously.
  • Subject with other significant uncontrolled medical illnesses that may interfere with drug administration or interpretation of results.
  • Subject who have been included in any other clinical trial within the previous 3 months.

Sites / Locations

  • Seberang Jaya Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Oil Palm Phenolics

Placebo

Arm Description

500 mg gallic acid equivalent (GAE), twice daily, 12 months

Placebo

Outcomes

Primary Outcome Measures

Blood Glucose Level
Serum Glycosylated Haemogoblin (<5.7% indicates healthy, 5.7% - 6.4% indicates prediabetes, >6.5% indicates diabetes) Plasma glucose level of oral glucose tolerance test (<7.8 mmol/L indicates healthy, 7.8 mmol/L - 11 mmol/L indicates prediabetes, >11 mmol/L indicates diabetes) Fasting plasma glucose level (<5.6 mmol/L indicates healthy, 5.6 mmol/L - 6.9 mmol/L indicates prediabetes, >6.9 mmol/L indicates diabetes)

Secondary Outcome Measures

Insulin Sensitivity
Model-derived Oral Glucose Insulin Sensitivity (OGIS) Index will be calculated using weight (kg), height (cm), glucose (mmol/L) and insulin (pmol/L).
Lipid profile
Total cholesterol, Low-density lipoprotein, High-density lipoprotein, Triglycerides
Global Assessment of Efficacy
Very good, good, no change, unsatisfactory and very unsatisfactory
Beta Cell Function
Homeostatic Model Assessment (HOMA2-B) to determine beta cell function

Full Information

First Posted
August 10, 2015
Last Updated
September 28, 2021
Sponsor
Universiti Sains Malaysia
Collaborators
Malaysia Palm Oil Board, Clinical Research Centre, Malaysia
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1. Study Identification

Unique Protocol Identification Number
NCT02532088
Brief Title
Modulating Effects of Oil Palm Phenolics in Subjects With Pre-diabetes
Acronym
PREDOPP
Official Title
Modulating Effects of Oil Palm Phenolics in Subjects With Pre-diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Withdrawn
Why Stopped
Project terminated
Study Start Date
May 2020 (Anticipated)
Primary Completion Date
June 2021 (Anticipated)
Study Completion Date
September 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universiti Sains Malaysia
Collaborators
Malaysia Palm Oil Board, Clinical Research Centre, Malaysia

4. Oversight

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

5. Study Description

Brief Summary
Study reported that providing Oil Palm Phenolics to Nile rats blocked diabetes progression in this spontaneous diabetes model. The present study aims to determine the beneficial effects of Oil Palm Phenolics in subjects with pre-diabetes.
Detailed Description
Recent studies suggest the potential of polyphenols as a supplementary treatment to delay or prevent the onset of diabetes owing to their biological properties. Polyphenols are natural phytochemical compounds found in fruits and vegetables. The most common group of phenolic compounds in our diet are phenolic acids and flavonoids. The two main classes are hydroxybenzoic acid derivatives and hydroxycinnamic acid derivatives. The anti-hyperglycemic property of polyphenols is mainly contributed by the reduction of dietary carbohydrate absorption through intestines, improvement of β-cell function and insulin action, stimulation of insulin secretion, modulation of the enzymes involved in glucose metabolism, anti-oxidative and anti-inflammatory effects. The key enzymes responsible for the digestion of dietary carbohydrates to glucose are α-glucosidase and α-amylase. One of the most well-known properties of polyphenols especially phenolic acids on carbohydrate metabolism is the inhibition of these enzymes. Some investigations have shown that polyphenols are also able to regulate postprandial glycemia and inhibit the development of glucose intolerance by a facilitated insulin response and increased secretion of glucose-dependent insulinotropic polypeptide (GIP) and glucagonlike polypeptide-1 (GLP-1). In addition, polyphenols are able to regulate the key pathways involved in carbohydrate metabolism and hepatic glucose homeostasis. These include glycolysis, glycogenesis and gluconeogenesis, which are usually impaired in diabetes. The current study focuses on the glucose-controlling properties of phenolic compounds extracted from oil palm (Elaeis guineensis), a high oil-producing tropical plant that also rich in phytochemicals. The major phenolic components in OPP are identified as caffeoylshikimic acid, protocatechuic acid and p-hydroxybenzoic acid. OPP has been found to exert various positive health effects parallel to the well-established physiological benefits of polyphenols. It has been shown that OPP protects against early type 2 diabetes and encouraging results suggest its role in modulating the development of diabetes. The current study aims to investigate and determine the effects of oil palm phenolics (OPP) on the blood glucose control in pre-diabetics.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prediabetes

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Oil Palm Phenolics
Arm Type
Active Comparator
Arm Description
500 mg gallic acid equivalent (GAE), twice daily, 12 months
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
Oil Palm Phenolics
Intervention Description
Palm fruit derived phenolics compound
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Blood Glucose Level
Description
Serum Glycosylated Haemogoblin (<5.7% indicates healthy, 5.7% - 6.4% indicates prediabetes, >6.5% indicates diabetes) Plasma glucose level of oral glucose tolerance test (<7.8 mmol/L indicates healthy, 7.8 mmol/L - 11 mmol/L indicates prediabetes, >11 mmol/L indicates diabetes) Fasting plasma glucose level (<5.6 mmol/L indicates healthy, 5.6 mmol/L - 6.9 mmol/L indicates prediabetes, >6.9 mmol/L indicates diabetes)
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Insulin Sensitivity
Description
Model-derived Oral Glucose Insulin Sensitivity (OGIS) Index will be calculated using weight (kg), height (cm), glucose (mmol/L) and insulin (pmol/L).
Time Frame
12 months
Title
Lipid profile
Description
Total cholesterol, Low-density lipoprotein, High-density lipoprotein, Triglycerides
Time Frame
12 months
Title
Global Assessment of Efficacy
Description
Very good, good, no change, unsatisfactory and very unsatisfactory
Time Frame
12 months
Title
Beta Cell Function
Description
Homeostatic Model Assessment (HOMA2-B) to determine beta cell function
Time Frame
12 months

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: Subject with "pre-diabetes", i.e. fasting plasma glucose level of more than 5.6 mmol/L and less than 7.0 mmol/L; or 2-hr plasma glucose load level of more than 7.8 mmol/L and less than 11.0 mmol/L. Subjects or his/her legally acceptable representative is willing to provide written informed consent. Exclusion Criteria: Subject with terminal cancer. Subject with renal failure (serum creatinine more than 200 umol/L). Subject with significant liver impairment (liver function test of 5 times more than the upper limit level). Subject with severe dementia and psychosis. Subject requires of long term corticosteroid treatment for the underlying disease such as connective tissue disorder. Subject with hemoglobinopathy or anemia. Subject underwent splenectomy or suffered from splenomegaly. Subject with pre-existing cardiovascular disease. Subject with chronic substance abuse such as chronic alcoholism or chronic opiate usage. Female subject of childbearing potential unless subject underwent bilateral tubal ligation, bilateral oophorectomy or hysterectomy previously. Subject with other significant uncontrolled medical illnesses that may interfere with drug administration or interpretation of results. Subject who have been included in any other clinical trial within the previous 3 months.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kah Hay Yuen, PhD
Organizational Affiliation
Universiti Sains Malaysia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Seberang Jaya Hospital
City
Seberang Jaya
State/Province
Penang
ZIP/Postal Code
13700
Country
Malaysia

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Modulating Effects of Oil Palm Phenolics in Subjects With Pre-diabetes

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