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NCT02146157 · ClinicalTrials.gov registry record · NA

Trial of an Herb and Mineral Combination Product on Fasting Glucose in Adults at Risk for Developing Diabetes

A NA study of PreDiabetes, sponsored by NewChapter.

Completed
Registry status
NA
Development phase
104
Enrollment target
6
Study locations

NCT02146157 is a NA study of PreDiabetes that has completed, run by NewChapter. The registered enrollment target is 104 participants, below the 690-participant average among 89 other PreDiabetes trials with a reported enrollment target (85% lower). The trial reports 6 study locations across 5 states.

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The verdict

NCT02146157, a NA study of PreDiabetes, has completed, sponsored by NewChapter.

COMPLETED
Registry status
NA
Development phase
104 participants
Enrollment target
6
Study locations

Study Summary

This is a multi-center, randomized, double-blind, placebo-controlled study in approximately 104 subjects (52 per group) to evaluate the effectiveness of an herb and mineral combination product on fasting serum glucose levels in subjects with impaired fasting glucose. The study consists of 5 visits: a Screening visit, followed by a Baseline visit (at which eligible subjects will be randomized to product to consume throughout the 12-week supplementation period), followed by Supplementation period visits at 3, 6 and 12 weeks after baseline.

Conditions Studied

Interventions

  • DIETARY_SUPPLEMENT Placebo
  • DIETARY_SUPPLEMENT herb and mineral combination product

Study Locations (6)

Ohio

  • Radiant Research - Cincinnati
  • Providence Health Partners Center for Clinical Research - Dayton

Illinois

  • Radiant Research - Chicago

Kentucky

  • Central Kentucky Research Associates - Lexington

Michigan

  • Quest Research Institute - Bingham Farms

South Carolina

  • Mountain View Clinical Research - Greer

Trial Details

FieldValue
Enrollment Target 104 participants
Start Date 2013-02
Est. Completion 2015-06
Phase NA

Sponsor

NewChapter

3 total trials

What the Registry Record Tells You About NCT02146157

The ClinicalTrials.gov registry entry for NCT02146157 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 104 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 690-participant average among 89 other PreDiabetes trials with a reported enrollment target (85% lower). The listed sponsor is NewChapter, which has 3 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with PreDiabetes appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT02146157 reports 6 study locations spanning 5 distinct geographic areas - top geographies include Ohio, Illinois, Kentucky.

Frequently Asked Questions

What is clinical trial NCT02146157 about?

NCT02146157 is a clinical study titled "Trial of an Herb and Mineral Combination Product on Fasting Glucose in Adults at Risk for Developing Diabetes". This is a multi-center, randomized, double-blind, placebo-controlled study in approximately 104 subjects (52 per group) to evaluate the effectiveness of an herb and mineral combination product on fasting serum glucose levels in subjects with impaired fasting glucose. The study consists of 5 visits: ...

What is the current status of trial NCT02146157?

This trial is currently completed. It is a NA study. The enrollment target is 104 participants. The study started on 2013-02. Estimated completion is 2015-06.

What conditions does trial NCT02146157 study?

This clinical trial studies the following conditions: PreDiabetes.

What interventions are being tested in trial NCT02146157?

The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), herb and mineral combination product (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT02146157?

This trial is sponsored by NewChapter, which has 3 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02146157 being conducted?

This trial has 6 study locations across Illinois, Kentucky, Michigan, Ohio, South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.