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Effects of D-allulose (Psicose) With Sucrose Beverage on Glucose Tolerance and Insulin Level

Primary Purpose

Impaired Glucose Tolerance

Status
Completed
Phase
Not Applicable
Locations
Thailand
Study Type
Interventional
Intervention
D-allulose
Sponsored by
Chiang Mai University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Impaired Glucose Tolerance

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Male or female, age > 18 years and legal age of consent.
  2. If female, the participant is either post-menopausal or surgically sterilized, or has a negative urine kit pregnancy test within 7 days prior to enrollment and will use adequate contraception during the study.
  3. The participant has provided written informed consent prior to admission to the study.
  4. Participant is able to join the entire study with 8 weeks.
  5. Participant is able to keep 24-hour dietary record a day prior to each visit.

Exclusion Criteria:

  1. Pregnancy or lactation
  2. Diagnosed with diabetes mellitus
  3. Those who take any medication that might be able to increase plasma glucose 1 month prior to the study or during in the study
  4. Acute illness within 1 weeks prior to the study
  5. Has gastrointestinal symptoms such as nausea, vomiting, loss of appetite, premature satiety, diarrhea, or chronic constipation
  6. Immunocompromised status, including a debilitated state or malignancy
  7. Active liver, renal, thyroid diseases
  8. Lack of ability or willingness to give informed consent
  9. Enrolled in any other clinical study within 3 months before enrolment
  10. Any people whose life style is irregular, for example, person works at night shifts.

Sites / Locations

  • Clinical trial Unit, Faculty of Medicine, Chiang Mai University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm Type

Placebo Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

Sucrose

SAlloulose2.5

SAllulose5

SAllulose7.5

SAllulose10

Arm Description

Sucrose 50 g

Sucrose 50 g + D-allulose (psicose) 2.5 g

Sucrose 50 g + D-allulose (psicose) 5 g

Sucrose 50 g + D-allulose (psicose) 7.5 g

Sucrose 50 g + D-allulose (psicose) 10 g

Outcomes

Primary Outcome Measures

The dose-response effects of D-allulose (psicose) with sucrose beverage on glucose tolerance
oral sucrose tolerance test with sucrose +/- allulose

Secondary Outcome Measures

Time to peak plasma glucose concentration
oral sucrose tolerance test with sucrose +/- allulose

Full Information

First Posted
February 23, 2015
Last Updated
January 30, 2016
Sponsor
Chiang Mai University
Collaborators
Kagawa University
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1. Study Identification

Unique Protocol Identification Number
NCT02455934
Brief Title
Effects of D-allulose (Psicose) With Sucrose Beverage on Glucose Tolerance and Insulin Level
Official Title
The Dose-response Effects of D-allulose (Psicose) With Sucrose Beverage on Glucose Tolerance and Insulin Level in Healthy Volunteers and Volunteers With Impaired Fasting Glucose
Study Type
Interventional

2. Study Status

Record Verification Date
January 2016
Overall Recruitment Status
Completed
Study Start Date
April 2015 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chiang Mai University
Collaborators
Kagawa University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Randomized, double-blind, crossover-trial, 30 subjects in each groups, either males or females, normal fasting glucose or pre-diabetes, aged > 18 years old to perform oral sucrose tolerance with either one of the 5 study products Sucrose 50 g Sucrose 50 g + D-allulose (psicose) 2.5 g Sucrose 50 g + D-allulose (psicose) 5 g Sucrose 50 g + D-allulose (psicose) 7.5 g Sucrose 50 g + D-allulose (psicose) 10 g Primary endpoints: To investigate the dose-response effects of D- allulose (psicose) with sucrose beverage on glucose tolerance To investigate the dose-response effects of D- allulose (psicose) with sucrose beverage on insulin levels
Detailed Description
Objectives Primary objectives To investigate the dose-response effects of D-allulose (psicose) with sucrose beverage on glucose tolerance To investigate the dose-response effects of D-allulose (psicose) with sucrose beverage on insulin levels Subjects and methods Study product A. Sucrose 50 g B. Sucrose 50 g + D-allulose (psicose) 2.5 g C. Sucrose 50 g + D-allulose (psicose) 5 g D. Sucrose 50 g + D-allulose (psicose) 7.5 g E. Sucrose 50 g + D-allulose (psicose) 10 g Study plan Screening (visit 0) Obtain inform consent History taking for medical problems, smoking, alcoholic drinking, concurrent medication, contraception or menopausal status, weight history Measure body weight, height and calculated BMI Measure waist and hip circumference Body composition measurement by bioelectrical impedance analysis (BIA) Complete physical examination Urine pregnancy test in all female of childbearing potential Provide 24-hour food record Ask to come back within 1 week Visit 1: (day 7 or 6-11 days) Complete physical examination Randomize subject to receive any 1 of 5 study products Perform OSTT with that product Return food record Provide 24-hour food record Adverse events evaluation Ask to come back within 7 +/- 4 days Visit 2: (day 7 or 6-11 days from visit 1) Complete physical examination Randomize subject to receive any 1 of 4 study product which are left Perform OSTT with that product Return food record Provide 24-hour food record Adverse events evaluation Ask to come back within 7 +/- 4 days Visit 3 (day 7 or 6-11 days from visit 2) Complete physical examination Randomize subject to receive any 1 of 3 study product which are left Perform OSTT with that product Return food record Provide 24-hour food record Adverse events evaluation Ask to come back within 7 +/- 4 days Visit 4 (day 7 or 6-11 days from visit 3) Complete physical examination Randomize subject to receive any 1 of 2 study product which are left Perform OSTT with that product Return food record Provide 24-hour food record Adverse events evaluation Ask to come back within 7 +/- 4 days Visit 5 (day 7 or 6-11 days from visit 4) Complete physical examination Perform OSTT with the product that is left Return food record Adverse events evaluation Adverse Event Assessment At each visit, participants will be asked an open question as if he/she has experienced any abnormal symptoms. Any symptom reported by the participants will be recorded as an adverse events with details of the event, its severity, start and stop dates, and relationship to study products. Gastrointestinal symptoms (heartburn, distension, nausea, vomiting, abdominal pain, flatulence, constipation and diarrhea) within 24 hours after OSTT will be asked and recorded as well. Withdrawal criteria Those who are not able to complete 5 visits of OSTT within 8 weeks Those who cannot provide 24-hour dietary record at each visit Those who start any medication that might cause increasing in plasma glucose during participating in the study

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Impaired Glucose Tolerance

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sucrose
Arm Type
Placebo Comparator
Arm Description
Sucrose 50 g
Arm Title
SAlloulose2.5
Arm Type
Active Comparator
Arm Description
Sucrose 50 g + D-allulose (psicose) 2.5 g
Arm Title
SAllulose5
Arm Type
Active Comparator
Arm Description
Sucrose 50 g + D-allulose (psicose) 5 g
Arm Title
SAllulose7.5
Arm Type
Active Comparator
Arm Description
Sucrose 50 g + D-allulose (psicose) 7.5 g
Arm Title
SAllulose10
Arm Type
Active Comparator
Arm Description
Sucrose 50 g + D-allulose (psicose) 10 g
Intervention Type
Dietary Supplement
Intervention Name(s)
D-allulose
Intervention Description
Eligible subjects will come for visit 1 to consume varying dose of D-allulose with sucrose beverage with 1 of 5 beverages in a random order which will be blinded for both subjects and investigators. They will have to do 24-hour dietary record a day prior to each visit. Subjects have to be abstained from energy diet within 8 hours prior to each visit. Venous blood samples will be collected 6 mL for measurement of FPG and insulin before taking any study product. Subjects have to drink all within 1 minute. Blood samples will be drawn again 6 mL at 30, 60, 90 and 120 min after consumption for measurement of PG and insulin. Every subject will be asked to come back to finish OSTT with 5 study products in a random order, each at 7 days or >5 days and <12 days apart.
Primary Outcome Measure Information:
Title
The dose-response effects of D-allulose (psicose) with sucrose beverage on glucose tolerance
Description
oral sucrose tolerance test with sucrose +/- allulose
Time Frame
2 hours
Secondary Outcome Measure Information:
Title
Time to peak plasma glucose concentration
Description
oral sucrose tolerance test with sucrose +/- allulose
Time Frame
2 hours
Other Pre-specified Outcome Measures:
Title
The dose-response effects of D-allulose with sucrose beverage on insulin levels after oral sucrose tolerance test
Description
Oral sucrose tolerance test with sucrose +/- allulose
Time Frame
2 hours
Title
Time to peak plasma insulin concentration
Description
Oral sucrose tolerance test with sucrose +/- allulose
Time Frame
2 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Male or female, age > 18 years and legal age of consent. If female, the participant is either post-menopausal or surgically sterilized, or has a negative urine kit pregnancy test within 7 days prior to enrollment and will use adequate contraception during the study. The participant has provided written informed consent prior to admission to the study. Participant is able to join the entire study with 8 weeks. Participant is able to keep 24-hour dietary record a day prior to each visit. Exclusion Criteria: Pregnancy or lactation Diagnosed with diabetes mellitus Those who take any medication that might be able to increase plasma glucose 1 month prior to the study or during in the study Acute illness within 1 weeks prior to the study Has gastrointestinal symptoms such as nausea, vomiting, loss of appetite, premature satiety, diarrhea, or chronic constipation Immunocompromised status, including a debilitated state or malignancy Active liver, renal, thyroid diseases Lack of ability or willingness to give informed consent Enrolled in any other clinical study within 3 months before enrolment Any people whose life style is irregular, for example, person works at night shifts.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Supawan Buranapin, MD
Organizational Affiliation
Chiang Mai University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinical trial Unit, Faculty of Medicine, Chiang Mai University
City
Muang
State/Province
ChiangMai
ZIP/Postal Code
50200
Country
Thailand

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
4299740
Citation
Cree GM, Perlin AS. O-isopropylidene derivatives of D-allulose (D-psicose) and D-erythro-hexopyranos-2,3-diulose. Can J Biochem. 1968 Aug;46(8):765-70. doi: 10.1139/o68-117. No abstract available.
Results Reference
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16232889
Citation
Takeshita K, Suga A, Takada G, Izumori K. Mass production of D-psicose from d-fructose by a continuous bioreactor system using immobilized D-tagatose 3-epimerase. J Biosci Bioeng. 2000;90(4):453-5. doi: 10.1016/s1389-1723(01)80018-9.
Results Reference
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16233597
Citation
Granstrom TB, Takata G, Tokuda M, Izumori K. Izumoring: a novel and complete strategy for bioproduction of rare sugars. J Biosci Bioeng. 2004;97(2):89-94. doi: 10.1016/S1389-1723(04)70173-5.
Results Reference
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PubMed Identifier
12026195
Citation
Matsuo T, Suzuki H, Hashiguchi M, Izumori K. D-psicose is a rare sugar that provides no energy to growing rats. J Nutr Sci Vitaminol (Tokyo). 2002 Feb;48(1):77-80. doi: 10.3177/jnsv.48.77.
Results Reference
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PubMed Identifier
19794929
Citation
Matsuo T, Izumori K. d-Psicose Inhibits Intestinal alpha-Glucosidase and Suppresses the Glycemic Response after Ingestion of Carbohydrates in Rats. J Clin Biochem Nutr. 2009 Sep;45(2):202-6. doi: 10.3164/jcbn.09-36. Epub 2009 Aug 28.
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PubMed Identifier
19155592
Citation
Iida T, Kishimoto Y, Yoshikawa Y, Hayashi N, Okuma K, Tohi M, Yagi K, Matsuo T, Izumori K. Acute D-psicose administration decreases the glycemic responses to an oral maltodextrin tolerance test in normal adults. J Nutr Sci Vitaminol (Tokyo). 2008 Dec;54(6):511-4. doi: 10.3177/jnsv.54.511.
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Citation
Hayashi N, Iida T, Yamada T, Okuma K, Takehara I, Yamamoto T, Yamada K, Tokuda M. Study on the postprandial blood glucose suppression effect of D-psicose in borderline diabetes and the safety of long-term ingestion by normal human subjects. Biosci Biotechnol Biochem. 2010;74(3):510-9. doi: 10.1271/bbb.90707. Epub 2010 Mar 7.
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Hossain A, Yamaguchi F, Matsunaga T, Hirata Y, Kamitori K, Dong Y, Sui L, Tsukamoto I, Ueno M, Tokuda M. Rare sugar D-psicose protects pancreas beta-islets and thus improves insulin resistance in OLETF rats. Biochem Biophys Res Commun. 2012 Sep 7;425(4):717-23. doi: 10.1016/j.bbrc.2012.07.135. Epub 2012 Aug 1.
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Ochiai M, Onishi K, Yamada T, Iida T, Matsuo T. D-psicose increases energy expenditure and decreases body fat accumulation in rats fed a high-sucrose diet. Int J Food Sci Nutr. 2014 Mar;65(2):245-50. doi: 10.3109/09637486.2013.845653. Epub 2013 Oct 21.
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Matsuo T, Izumori K. Effects of dietary D-psicose on diurnal variation in plasma glucose and insulin concentrations of rats. Biosci Biotechnol Biochem. 2006 Sep;70(9):2081-5. doi: 10.1271/bbb.60036. Epub 2006 Sep 7.
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Citation
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Effects of D-allulose (Psicose) With Sucrose Beverage on Glucose Tolerance and Insulin Level

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