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PrediabetesPhase 2NCT01554020

Blood Sugar Take Care and Glucose Metabolism

A Phase 2 study testing Blood Sugar Take Care in people with Prediabetes, run by NewChapter, Inc. at 1 site in United States.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

This prospective international clinical trial is a two-arm, double-blind, randomized, placebo-controlled, parallel-group, multicenter study. 112 prediabetic subjects will be randomized to Blood Sugar Take Care or placebo. Randomization will be stratified by gender. The intervention period is 12 weeks. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Prediabetes
What is being tested?
Blood Sugar Take Care
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
0 participants
Where
1 siteUnited States
Study dates
Jun 2012to Nov 2013
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

SUBJECT INCLUSION CRITERIA: STEP 1

  1. Age ≥ 18 years
  2. Subject meets American Diabetes Association criteria for diabetes testing in asymptomatic, undiagnosed individuals:
  3. If age ≥45 years, subject must have a body mass index ≥ 25 kg/m2 for United States and ≥ 24 kg/m2 for Indonesia
  4. If age <45 years, subject must have a body mass index ≥ 25 kg/m2 for United States and ≥ 24 kg/m2 for Indonesia AND present with at least one of the following risk factors:
  • Have a first-degree relative with diabetes
  • Habitually physically inactive
  • Race is African-American, Hispanic American, Native American, Asian American, or Pacific Islander
  • Have delivered a baby weighing >9 lb or have been diagnosed with gestational diabetes mellitus
  • Hypertensive (≥140/90)
  • Known HDL cholesterol level 35 mg/dl
  • Known triglyceride level ≥250 mg/dl
  • On previous testing, had impaired glucose tolerance or impaired fasting glucose
  • History of vascular disease
  1. Stable body weight (<5% change) in the last 3 months
  2. Agree to use contraception throughout study period, unless postmenopausal or surgically sterile (females only)
  3. Able to understand the nature and purpose of the study including potential risks and side effects
  4. Willing to consent to study participation and to comply with study requirements

SUBJECT EXCLUSION CRITERIA

  1. Known diabetes (type I or II)
  2. Recent use (within 2 weeks of screening) of any dietary supplement including vitamin and mineral complexes; herbal supplements; fish oil; fiber supplements; or any herbal ingredient/product that significantly affects glucose or lipid metabolism
  3. Recent use (within 4 weeks of screening) of any prescription or OTC medication that significantly affects glucose or lipid metabolism, including but not limited to, sulfonylureas, meglitinides, biguanides, thiazolidinediones, alpha-glucosidase inhibitors, DPP-4 inhibitors, systemic corticosteroids, statins, fibrates, niacin, and bile acid sequestrants
  4. Daily use of nonsteroidal anti-inflammatory drugs (NSAIDS); (daily baby aspirin use acceptable)
  5. Any comorbidity 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
  6. Anticipated changes in dietary patterns or physical activity levels during the study, including attempts at body weight reduction
  7. Eating disorder
  8. Polycystic ovary syndrome
  9. Known allergies to any substance in the study product
  10. Pregnant or breastfeeding women
  11. History of alcohol, drug, or medication abuse
  12. Participation in another study with any investigational product within 3 months of screening
  13. Recent (<3 months) gastrointestinal surgery or any planned surgery during the treatment period

SUBJECT INCLUSION CRITERIA: STEP 2

  1. Fasting glucose between 95 and 130 mg/dl, based on portable glucometer reading

SUBJECT INCLUSION CRITERIA: STEP 3

  1. Impaired fasting glucose, based on the American Diabetes Association definition of fasting serum glucose between 100 and 125 mg/dl
  2. Impaired glucose tolerance, based on the American Diabetes Association definition of serum glucose between 140 and 199 mg/dl 2 hours after a 75 g glucose load

Trial locations and contacts

1 site in 1 country.

United States1 site
  • SPRIM

    San Francisco, California, 94109

Other trials in United States

About this study

Official title: Effect of Blood Sugar Take Care on Glucose Metabolism, Determinants of Metabolic Syndrome, and Quality of Life in Prediabetic Adults: A Randomized, Double-blind, Placebo-controlled Study

This prospective international clinical trial is a two-arm, double-blind, randomized, placebo-controlled, parallel-group, multicenter study. 112 prediabetic subjects will be randomized to Blood Sugar Take Care or placebo. Randomization will be stratified by gender. The intervention period is 12 weeks. The primary outcome is fasting glucose levels.

Conditions
Prediabetes
Being tested
Blood Sugar Take Care, Placebo
Keywords
Blood glucose, Insulin sensitivity, Oral glucose tolerance
Medical subject headings
Prediabetic State, Insulin Resistance

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Blood Sugar Take CareDietary supplement

    Also called BSTC

    One 1200 mg soft gel capsule administered 3X/day for duration of study

  • PlaceboDietary supplement

    One 1200 mg soft-gel capsule administered 3X/day for duration of study

Study groups in NCT01554020
Study groupRoleWhat they receive
Multiherb productActive comparatorHerbal product
Receives: Dietary Supplement: Blood Sugar Take Care
PlaceboPlacebo comparatorMaltodextrin control
Receives: Dietary Supplement: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Fasting glucose

    Measured: 12 weeks

Secondary outcomes (17)
  1. Insulin sensitivity index

    Measured: 12 weeks

  2. Fasting insulin

    Measured: 12 weeks

  3. Homeostasis Model Assessment of Insulin Resistance

    Measured: 12 weeks

  4. Quantitative insulin sensitivity check index

    Measured: 12 weeks

  5. Insulin secretion/insulin resistance index

    Measured: 12 weeks

  6. Glycosylated hemoglobin (HbA1c)

    Measured: 12 weeks

  7. High-sensitivity C-reactive protein

    Measured: 12 weeks

  8. High-molecular weight adiponectin

    Measured: 12 weeks

  9. Lipids (total cholesterol, HDL, LDL, VLDL, triglycerides)

    Measured: 12 weeks

  10. Body composition

    height/weight, body mass index, waist circumference, hip circumference, waist-to-hip ratio

    Measured: 12 weeks

  11. WHO Quality of Life Questionnaire

    Measured: 12 weeks

  12. Comprehensive metabolic panel

    Measured: 12 weeks

  13. Complete blood count

    Measured: 12 weeks

  14. Adverse events

    Measured: 12 weeks

  15. Gastrointestinal Symptom Rating Scale

    Measured: 12 weeks

  16. Pulse

    Measured: 12 weeks

  17. Blood pressure

    Measured: 12 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Mar 2012 (estimated)
  2. Study startJun 2012
  3. Primary completionOct 2013 (estimated)
  4. Study completionNov 2013 (estimated)

Why it stopped: Change of CRO

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01554020
Sponsor's protocol ID
120216-SUS-NWC-BSS-GP
Status last verified
Mar 2013
First submitted
7 Mar 2012
Last updated
12 Mar 2013
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Blood Sugar Take Care in people with Prediabetes, run by NewChapter, Inc. at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 12 Mar 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Fasting glucose (time frame: 12 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Mar 2013.

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