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NCT03844503 · ClinicalTrials.gov registry record · NA

Food Containing Resistant Starch Type 4 and Postprandial Glycemic Response

A NA study of Healthy, sponsored by Clinical Nutrition Research Center, Illinois Institute of Technology.

Completed
Registry status
NA
Development phase
31
Enrollment target
1
Study location

NCT03844503 is a NA study of Healthy that has completed, run by Clinical Nutrition Research Center, Illinois Institute of Technology. The registered enrollment target is 31 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03844503, a NA study of Healthy, has completed, sponsored by Clinical Nutrition Research Center, Illinois Institute of Technology.

COMPLETED
Registry status
NA
Development phase
31 participants
Enrollment target
1
Study location

Study Summary

The primary objective of the study is to determine if resistant starch reduces the 2 hour glycemic response as measured by positive incremental area under the blood glucose response curve (Positive iAUC- ignores area below fasting). Secondary endpoints include insulin iAUC, glucose and insulin net incremental AUC (net iAUC), time point of peak rise (T max) of glucose and insulin, and glucose and insulin concentrations at each time point (C max).

Conditions Studied

Healthy

Interventions

  • DIETARY_SUPPLEMENT Cereal Bar no fiber
  • DIETARY_SUPPLEMENT Cereal bar with 10 g fiber
  • DIETARY_SUPPLEMENT Cereal bar with 20 g fiber

Study Locations (1)

Illinois

  • Clinical Nutrition Research Center - Chicago

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2019-02-11
Est. Completion 2019-10-25
Phase NA

Sponsor

Clinical Nutrition Research Center, Illinois Institute of Technology

59 total trials

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What the Registry Record Tells You About NCT03844503

The ClinicalTrials.gov registry entry for NCT03844503 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (95% lower). The listed sponsor is Clinical Nutrition Research Center, Illinois Institute of Technology, which has 59 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Healthy appearing as the primary indexed condition, and to 3 interventions - of which Cereal Bar no fiber is the first listed.

NCT03844503 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.

Frequently Asked Questions

What is clinical trial NCT03844503 about?

NCT03844503 is a clinical study titled "Food Containing Resistant Starch Type 4 and Postprandial Glycemic Response". The primary objective of the study is to determine if resistant starch reduces the 2 hour glycemic response as measured by positive incremental area under the blood glucose response curve (Positive iAUC- ignores area below fasting). Secondary endpoints include insulin iAUC, glucose and insulin net i...

What is the current status of trial NCT03844503?

This trial is currently completed. It is a NA study. The enrollment target is 31 participants. The study started on 2019-02-11. Estimated completion is 2019-10-25.

What conditions does trial NCT03844503 study?

This clinical trial studies the following conditions: Healthy.

What interventions are being tested in trial NCT03844503?

The interventions under investigation include: Cereal Bar no fiber (DIETARY_SUPPLEMENT), Cereal bar with 10 g fiber (DIETARY_SUPPLEMENT), Cereal bar with 20 g fiber (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT03844503?

This trial is sponsored by Clinical Nutrition Research Center, Illinois Institute of Technology, which has 59 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03844503 being conducted?

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

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