To Evaluate the Impact of Consumption of a Bioactive Compound on Fasting Blood Glucose Levels in Asian Indians With Pre-diabetes

NCT06417840 | Recruiting

• 1 other identifier: 1.4/FCDOC/EC/HAO/2024-25
• Study Type: interventional
• Target: 130
• Locations: 1 country
• Sites: 1

Brief Summary

This is randomized placebo controlled, double-blinded, parallel arm study on free living Asian Indians. Eligible subjects will undergo one-week run-in period and subjects will be asked to maintain their usual diet and exercise regime. At the end of the run-in period, subjects fulfilling the inclusion/exclusion criteria at this stage will be randomized either to the intervention arm or control arm using computerized random number tables. The measured parameters will include, 24-h diet recall, food frequency questionnaire, anthropometry including circumferences, height and weight, and blood parameters including blood glucose (fasting), serum insulin (fasting), HbA1c and lipid profile.

Conditions

PreDiabetes

Outcome Measures

Primary Outcomes (1)

• Fasting Blood Glucose

  Blood Glucose Concentration mg/dL

  0, and 28 days

Secondary Outcomes (11)

• Fasting Blood Insulin

  0, and 28 days

• HbA1c

  0, and 28 days

• Continuous Glucose Monitoring

  0, and 28 days

• Total Cholesterol

  0, and 28 days

• Low-density lipoprotein (LDL) cholesterol

  0, and 28 days

Study Arms (2)

Placebo Control

PLACEBO COMPARATOR

Dietary Supplement: Placebo Control

N-trans-caffeoyltyramine (NCT) and N-trans-feruloyltyramine (NFT)

EXPERIMENTAL

Dietary Supplement: N-trans-caffeoyltyramine (NCT) and N-trans-feruloyltyramine (NFT)

Interventions

N-trans-caffeoyltyramine (NCT) and N-trans-feruloyltyramine (NFT) DIETARY_SUPPLEMENT

N-trans-caffeoyltyramine (NCT) and N-trans-feruloyltyramine (NFT) derived via synthetic biology (i.e., fermentation using a recombinant microorganism) to provide a high purity (\>85%) form of these compounds that are structurally identical to their naturally occurring counterparts. All ingredients in the encapsulated final test article, including the NCT and NFT, are manufactured under food GMPs and are of suitable quality for use in food, dietary supplements, and specialty nutrition products.

N-trans-caffeoyltyramine (NCT) and N-trans-feruloyltyramine (NFT)

Placebo Control DIETARY_SUPPLEMENT

Placebo Control

Placebo Control

Eligibility Criteria

• Age: 18 Years - 50 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Fasting Blood Glucose between 100-125 mg/dL;
• and BMI range 25-30 kg/m2;
• and waist circumference ≥80cm for women and ≥90cm for men;

You may not qualify if:

• Weight loss or gain ≥4.5 kg within 90 days of visit 1.
• Use of weight loss medications within 90 days of visit 1.
• History of gastrointestinal surgery (e.g., bariatric surgery) or cosmetic procedures (e.g., liposuction) for weight/fat reducing purposes.
• Use of dietary supplements or related products that, in the judgment of the Investigator, are likely to markedly affect weight loss or appetite within 30 days of visit 1.
• History of extreme dietary habits (e.g., Atkins diet, etc.), as judged by the Investigator.
• History of an eating disorder (e.g., anorexia nervosa, bulimia nervosa, or binge eating) diagnosed by a health professional.
• Current medical diagnosis of type 1 or type 2 diabetes mellitus.
• HbA1c ≥48 mmol/mol (6.5%) as measured at visit 1.
• History of a chronic gastrointestinal disorder, such as peptic ulcer disease or malabsorption syndrome (mild lactose intolerance or gastroesophageal reflux diseases are acceptable).
• Signs or symptoms of an active infection of clinical relevance within 5 days of visit 1. The visit may be rescheduled such that all signs and symptoms have resolved (at the discretion of the Clinical Investigator) at least 5 days prior to visit 1.
• Is pregnant, planning to be pregnant during the study period, lactating, or is of childbearing potential and is unwilling to commit to the use of a medically approved form of contraception throughout the study period. The method of contraception must be recorded in the source document.
• Any condition the Investigator believes would interfere with his or her ability to provide informed consent, comply with the study protocol, or which might confound the interpretation of the study results or put the person at undue risk.
• Excessive alcohol consumption (\> 2 Drinks, 60 ml of Whisky Per Day).

Sponsors & Collaborators

• Brightseed: lead

Study Sites (1)

Diabetes Foundation (India)

New Delhi, 110 016, India

RECRUITING

MeSH Terms

Conditions

Prediabetic State

Condition Hierarchy (Ancestors)

Diabetes Mellitus; Glucose Metabolism Disorders; Metabolic Diseases; Nutritional and Metabolic Diseases; Endocrine System Diseases

Central Study Contacts

Anoop Misra, PhD

CONTACT

91-11-41759672; anoopmisra@gmail.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: May 13, 2024
• First Posted: May 16, 2024
• Study Start: June 22, 2024
• Primary Completion: October 30, 2024
• Study Completion: October 30, 2024
• Last Updated: July 24, 2024

Record last verified: 2024-07

Locations

IN (1)