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.
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
- Age ≥ 18 years
- Subject meets American Diabetes Association criteria for diabetes testing in asymptomatic, undiagnosed individuals:
- If age ≥45 years, subject must have a body mass index ≥ 25 kg/m2 for United States and ≥ 24 kg/m2 for Indonesia
- 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
- Stable body weight (<5% change) in the last 3 months
- Agree to use contraception throughout study period, unless postmenopausal or surgically sterile (females only)
- Able to understand the nature and purpose of the study including potential risks and side effects
- Willing to consent to study participation and to comply with study requirements
SUBJECT EXCLUSION CRITERIA
- Known diabetes (type I or II)
- 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
- 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
- Daily use of nonsteroidal anti-inflammatory drugs (NSAIDS); (daily baby aspirin use acceptable)
- 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
- 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 to any substance in the study product
- Pregnant or breastfeeding women
- History of alcohol, drug, or medication abuse
- Participation in another study with any investigational product within 3 months of screening
- Recent (<3 months) gastrointestinal surgery or any planned surgery during the treatment period
SUBJECT INCLUSION CRITERIA: STEP 2
- Fasting glucose between 95 and 130 mg/dl, based on portable glucometer reading
SUBJECT INCLUSION CRITERIA: STEP 3
- Impaired fasting glucose, based on the American Diabetes Association definition of fasting serum glucose between 100 and 125 mg/dl
- 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.
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 group | Role | What they receive |
|---|---|---|
| Multiherb product | Active comparator | Herbal product Receives: Dietary Supplement: Blood Sugar Take Care |
| Placebo | Placebo comparator | Maltodextrin control Receives: Dietary Supplement: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Fasting glucose
Measured: 12 weeks
Secondary outcomes (17)
Insulin sensitivity index
Measured: 12 weeks
Fasting insulin
Measured: 12 weeks
Homeostasis Model Assessment of Insulin Resistance
Measured: 12 weeks
Quantitative insulin sensitivity check index
Measured: 12 weeks
Insulin secretion/insulin resistance index
Measured: 12 weeks
Glycosylated hemoglobin (HbA1c)
Measured: 12 weeks
High-sensitivity C-reactive protein
Measured: 12 weeks
High-molecular weight adiponectin
Measured: 12 weeks
Lipids (total cholesterol, HDL, LDL, VLDL, triglycerides)
Measured: 12 weeks
Body composition
height/weight, body mass index, waist circumference, hip circumference, waist-to-hip ratio
Measured: 12 weeks
WHO Quality of Life Questionnaire
Measured: 12 weeks
Comprehensive metabolic panel
Measured: 12 weeks
Complete blood count
Measured: 12 weeks
Adverse events
Measured: 12 weeks
Gastrointestinal Symptom Rating Scale
Measured: 12 weeks
Pulse
Measured: 12 weeks
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.
- First posted14 Mar 2012 (estimated)
- Study startJun 2012
- Primary completionOct 2013 (estimated)
- Study completionNov 2013 (estimated)
Why it stopped: Change of CRO
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for PrediabetesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- NewChapter, Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Sprim Advanced Life Sciences
- Responsible party
- Sponsor
- Investigators
- Larry Miller, PhD, Principal investigator, Sprim Advanced Life Sciences
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
Study at a glance
From the registry record, last updated by the sponsor on 12 Mar 2013. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT01554020
- Acronym / sponsor ID
- 120216-SUS-NWC-BSS-GP
- Conditions
- Prediabetes
- Keywords
- Blood glucose, Insulin sensitivity, Oral glucose tolerance
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- WithdrawnReason stopped: Change of CRO
- Enrolment
- 0 participants (actual)
- Lead sponsor
- NewChapter, Inc.Industry (pharma, biotech, devices)
- Collaborators
- Sprim Advanced Life Sciences
- Study start
- Jun 2012
- Primary completion
- Oct 2013 (estimated)
- Study completion
- Nov 2013 (estimated)
- First posted
- 14 Mar 2012 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Multiherb product | Active comparator | Dietary Supplement: Blood Sugar Take CareHerbal product |
| Placebo | Placebo comparator | Dietary Supplement: PlaceboMaltodextrin control |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Blood Sugar Take CareAlso: BSTCOne 1200 mg soft gel capsule administered 3X/day for duration of study | Dietary supplement | Multiherb product |
| PlaceboOne 1200 mg soft-gel capsule administered 3X/day for duration of study | Dietary supplement | Placebo |
Primary outcome
Fasting glucose
Time frame: 12 weeks
17 secondary outcomes
Insulin sensitivity index
Time frame: 12 weeks
Fasting insulin
Time frame: 12 weeks
Homeostasis Model Assessment of Insulin Resistance
Time frame: 12 weeks
Quantitative insulin sensitivity check index
Time frame: 12 weeks
Insulin secretion/insulin resistance index
Time frame: 12 weeks
Glycosylated hemoglobin (HbA1c)
Time frame: 12 weeks
High-sensitivity C-reactive protein
Time frame: 12 weeks
High-molecular weight adiponectin
Time frame: 12 weeks
Lipids (total cholesterol, HDL, LDL, VLDL, triglycerides)
Time frame: 12 weeks
Body composition
Time frame: 12 weeks
WHO Quality of Life Questionnaire
Time frame: 12 weeks
Comprehensive metabolic panel
Time frame: 12 weeks
Complete blood count
Time frame: 12 weeks
Adverse events
Time frame: 12 weeks
Gastrointestinal Symptom Rating Scale
Time frame: 12 weeks
Pulse
Time frame: 12 weeks
Blood pressure
Time frame: 12 weeks
Results and safety
The study was withdrawn before enrolling participants, so there are no results.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Mar 2013.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Larry Miller, PhD principal investigator
Sprim Advanced Life Sciences
1 site in 1 country: see every site and its status.
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.