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

Not Applicable

Completed

• Conditions: Prediabetes

• Registration Number: NCT02146157
• Lead Sponsor: NewChapter, Inc.

Brief 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.

Detailed Description

The target population of this clinical trial is otherwise healthy, pre-diabetic adults who present with impaired fasting glucose.

Study Timeline

• Study Start: 2013-02
• Study First Submitted: 2014-04-07
• Study First Submitted QC: 2014-05-20
• Study First Posted: 2014-05-23
• Primary Completion: 2015-06
• Study Completion: 2015-06
• Status Verified: 2015-10
• Last Update Submitted: 2015-10-12
• Last Update Posted: 2015-10-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 104

Inclusion Criteria

• Be male or female, at least 18 years of age
• If age ≥45 years, must have a body mass index ≥ 25 kg/m2
• If age <45 years, must have a body mass index ≥ 25 kg/m2 AND present with at least one additional risk factors for developing diabetes.
• Agree to use contraception throughout study period, unless postmenopausal or surgically sterile (women only)
• Be able to understand the nature and purpose of the study including potential risks and side effects
• Be willing to consent to study participation and to comply with study requirements
• Have a finger stick fasting blood glucose between 105 and 140 mg/dL and a serum fasting glucose between 100 and 125 mg/dL, measured at screening

Exclusion Criteria

• Have diabetes (type I or II) or an HBA1c measurement >6.5% at any time in the past or at the screening visit
• Have been taking within 2 weeks of screening any dietary supplement including vitamin and mineral complexes; herbal supplements; fish oil; fiber supplements; or any herbal ingredient/product that significantly affects glucose metabolism
• Have been taking within 4 weeks of screening any prescription or over-the-counter (OTC) medication that significantly affects glucose metabolism, including but not limited to, sulfonylureas, meglitinides, biguanides, thiazolidinediones, alpha-glucosidase inhibitors, Inhibitors of dipeptidyl peptidase 4 (DPP-4 inhibitors), systemic corticosteroids
• Daily use of non-steroidal anti-inflammatory drugs (NSAIDS) (daily baby aspirin use and continuous use of NSAIDS for 3 days or less for acute aches and pains are acceptable)
• Any co-morbidity or treatment that could, in the opinion of the investigator, preclude the subject's ability to successfully and safely complete the study or that may confound study outcomes
• Anticipated changes in dietary patterns or physical activity levels during the study, including attempts at body weight reduction
• Eating disorder
• Polycystic ovary syndrome
• Known allergies or intolerance to any substance in the study product
• Are pregnant or breastfeeding women
• History of alcohol, drug, or medication abuse
• Have participated in another study with any investigational product within 1 month of screening
• Had a recent (<3 months) gastrointestinal surgery or any planned surgery during the clinical study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Change from Baseline in fasting blood glucose	Day 84	Fasting glucose will be measured on serum samples obtained at screening (to be used as baseline value) and at day 84

Secondary Outcome Measures

Name	Time	Method
Change from Baseline in fasting serum glucose	Day 42	Fasting glucose will be measured on serum samples obtained at screening (to be used as baseline value) and at day 42
Change from Baseline in fasting blood glucose	Day 21	Fasting glucose will be measured on serum samples obtained at screening (to be used as baseline value) and at day 21
Change from Baseline in HbA1c	Day 84	Glycosylated hemoglobin (HbA1c) will be measured on whole blood samples obtained at screening and at day 84.
Change from Baseline in fasting lipids	Day 21	Total cholesterol, high-density lipoprotein, low-density lipoprotein, very low-density lipoprotein, and triglycerides will be measured on serum samples obtained at screening and at day 21 using a standard lipid panel.
Change from Baseline in BMI	Day 84	Body mass index
Change from Baseline in waist-to-hip ratio	Day 84

Trial Locations

Locations (5)

Radiant Research; 🇺🇸 Cincinnati, Ohio, United States

Central Kentucky Research Associates; 🇺🇸 Lexington, Kentucky, United States

Quest Research Institute; 🇺🇸 Bingham Farms, Michigan, United States

Providence Health Partners Center for Clinical Research; 🇺🇸 Dayton, Ohio, United States

Mountain View Clinical Research; 🇺🇸 Greer, South Carolina, United States