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NCT02714413 · ClinicalTrials.gov registry record · Phase 2

Effect of D-allulose in Addition to Oral Sucrose Load

A Phase 2 study of Blood Glucose, sponsored by University of Florida.

Completed
Registry status
Phase 2
Development phase
50
Enrollment target
1
Study location

NCT02714413: Completed Phase 2 study of Blood Glucose, sponsored by University of Florida.

NCT02714413 is a Phase 2 study of Blood Glucose that has completed, run by University of Florida. The registered enrollment target is 50 participants, roughly in line with the 50-participant average among 4 other Blood Glucose trials with a reported enrollment target. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02714413, a Phase 2 study of Blood Glucose, has completed, sponsored by University of Florida.

COMPLETED
Registry status
Phase 2
Development phase
50 participants
Enrollment target
1
Study location

Study Summary

Individuals in the United States now consume a substantial proportion of their total energy as added sugars. The consumption of caloric sweeteners has been steadily increasing over the last four decades. The potential health consequences of this practice have been subject to considerable debate. In addition to weight gain, higher consumption of sugar-sweetened beverages is associated with development of metabolic syndrome and type 2 diabetes. These findings support the current dietary guidelines that encourage consumers to limit their intake of added sugars. There is a need for a sugar substitute that is safe, palatable and has favorable effects on energy metabolism and overall glucose homeostasis. One such sugar is possibly D-allulose also referred to in the literature as D-psicose. The present proposal is to address the efficacy of D-allulose in reducing postprandial blood glucose level in a random sample of Caucasian and African American population. Specifically the effect of D-allulose ingestion on the glucose and insulin response to a standardized oral glucose load will be studied.

Primary Outcome

Evaluation of the efficacy of pure D-allulose on the glycemic excursion following a standard oral sucrose load.

Conditions Studied

Interventions

  • OTHER Placebo
  • DIETARY_SUPPLEMENT D-allulose
  • DIETARY_SUPPLEMENT sucrose

Study Locations (1)

Florida

  • University of Florida - Jacksonville

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2016-08
Est. Completion 2017-06-30
Phase Phase 2
University of Florida

1,106 total trials

What the finished NCT02714413 record still lists

NCT02714413 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, roughly in line with the 50-participant average among 4 other Blood Glucose trials with a reported enrollment target.

The record links to 1 condition, with Blood Glucose appearing as the primary indexed condition, and to 3 interventions - of which Placebo is the first listed.

NCT02714413 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT02714413 about?

NCT02714413 is a clinical study titled "Effect of D-allulose in Addition to Oral Sucrose Load". Individuals in the United States now consume a substantial proportion of their total energy as added sugars. The consumption of caloric sweeteners has been steadily increasing over the last four decades. The potential health consequences of this practice have been subject to considerable debate. In ...

What is the current status of trial NCT02714413?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 50 participants. The study started on 2016-08. Estimated completion is 2017-06-30.

What conditions does trial NCT02714413 study?

This clinical trial studies the following conditions: Blood Glucose.

What interventions are being tested in trial NCT02714413?

The interventions under investigation include: Placebo (OTHER), D-allulose (DIETARY_SUPPLEMENT), sucrose (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT02714413?

This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02714413 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT02714413, the US trial registry maintained by the National Library of Medicine. NCT02714413 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.