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NCT03388762 · ClinicalTrials.gov registry record · NA

RCT of a Polyherbal Dietary Supplement for Prediabetes

A NA study of Prediabetic State, sponsored by University of Maryland, Baltimore.

Completed
Registry status
NA
Development phase
39
Enrollment target
4
Study locations

NCT03388762 is a NA study of Prediabetic State that has completed, run by University of Maryland, Baltimore. The registered enrollment target is 39 participants, below the 603-participant average among 21 other Prediabetic State trials with a reported enrollment target (94% lower). The trial reports 4 study locations across 2 states.

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The verdict

NCT03388762, a NA study of Prediabetic State, has completed, sponsored by University of Maryland, Baltimore.

COMPLETED
Registry status
NA
Development phase
39 participants
Enrollment target
4
Study locations

Study Summary

The primary purpose of this study is to evaluate the impact of a polyherbal dietary supplement (Designs for Health - GlucoSupreme™ Herbal) on markers of glycemic control and other structure/function outcomes among a sample of prediabetic adults. A 12-week randomized, double-blinded, placebo-controlled clinical trial will be conducted to achieve the purpose of this study. The research team hypothesizes that GlucoSupreme™ Herbal will improve a variety of validated markers of glycemic control that are commonly used in clinical practice more effectively than placebo.

Conditions Studied

Interventions

  • OTHER Placebo
  • DIETARY_SUPPLEMENT GlucoSupreme™ Herbal

Study Locations (4)

Maryland

  • University of Maryland Center for Diabetes and Endocrinology - Baltimore
  • University of Maryland Family Medicine Associates - Baltimore
  • University of Maryland School of Medicine, Department of Family and Community Medicine, East Hall - Baltimore

Ohio

  • Alliance Integrative Medicine - Cincinnati

Trial Details

FieldValue
Enrollment Target 39 participants
Start Date 2017-12-05
Est. Completion 2020-01-01
Phase NA

Sponsor

University of Maryland, Baltimore

560 total trials

What the Registry Record Tells You About NCT03388762

The ClinicalTrials.gov registry entry for NCT03388762 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 39 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 603-participant average among 21 other Prediabetic State trials with a reported enrollment target (94% lower). The listed sponsor is University of Maryland, Baltimore, which has 560 total studies on file at ClinicalTrials.gov.

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

NCT03388762 reports 4 study locations spanning 2 distinct geographic areas - top geographies include Maryland, Ohio.

Frequently Asked Questions

What is clinical trial NCT03388762 about?

NCT03388762 is a clinical study titled "RCT of a Polyherbal Dietary Supplement for Prediabetes". The primary purpose of this study is to evaluate the impact of a polyherbal dietary supplement (Designs for Health - GlucoSupreme™ Herbal) on markers of glycemic control and other structure/function outcomes among a sample of prediabetic adults. A 12-week randomized, double-blinded, placebo-control...

What is the current status of trial NCT03388762?

This trial is currently completed. It is a NA study. The enrollment target is 39 participants. The study started on 2017-12-05. Estimated completion is 2020-01-01.

What conditions does trial NCT03388762 study?

This clinical trial studies the following conditions: Prediabetic State.

What interventions are being tested in trial NCT03388762?

The interventions under investigation include: Placebo (OTHER), GlucoSupreme™ Herbal (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT03388762?

This trial is sponsored by University of Maryland, Baltimore, which has 560 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03388762 being conducted?

This trial has 4 study locations across Maryland, Ohio. 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 Editorial

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.