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Efficacy of fiber-multivitamin combination on glycemic control, lipid profiles and body composition in overweight/obese adults with impaired fasting glucose.

Efficacy of fiber-multivitamin combination on glycemic control, lipid profiles and body composition in overweight/obese adults with impaired fasting glucose.

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20180618001
Enrollment
80
Registered
2018-06-18
Start date
2018-07-02
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes is a major social burden. In 2017&#44

Interventions

Oat fiber,Fibersol
Experimental Dietary Supplement,Placebo Comparator No treatment

Sponsors

Unicity Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0 Years to 0 Years

Inclusion criteria

Inclusion criteria: -BMI 23-35 kg/m2 -waist circumference > 80 cm in female or > 90 cm in male -Impaired fasting glucose screening by * fasting blood glucose levels between 6.1 and 7.0 mmol/L (110 and 125 mg/dL) * 2-hour Glucose Tolerance Test with 75 g of oral glucose dose, blood plasma glucose between 7.8 mmol/L (140 mg/dL) and 11.1 mmol/L (200 mg/dL) -No anti-diabetic and lipid-lowering therapy -Stable body weight for at least 6 mo

Exclusion criteria

Exclusion criteria: -Pregnant or lactating females -Persons with known allergies to any ingredients in either the active or placebo study compounds will be also excluded. -People who habitually used a dietary fiber supplement will be also excluded. -Following, or recently followed, a diet plan or supplement or medication use known to affect the trial - Anyone who has had a history of diagnosed type 2 diabetes mellitus, gastrointestinal disease, poorly controlled hypertension (systolic blood pressure > 160 mmHg, diastolic blood pressure > 100 mmHg), renal disease, liver disease, and thyroid disease, as well as severe health condition (e.g., cancer, cardiovascular disease). - participating in any vigorous exercise program

Design outcomes

Primary

MeasureTime frame
fasting blood glucose 12 weeks after end of the intervention the automated (enzymatic) method

Secondary

MeasureTime frame
fasting insulin 12 weeks after end of the intervention Chemiluminescence immunoassay (CLIA),blood lipid profiles 12 weeks after end of the intervention Enzymatic colorimetric method,% body fat (body composition) 12 weeks after end of the intervention DXA (Dual X-ray absorptometry)

Countries

Thailand

Contacts

Public ContactWantanee Kriengsinyos

Institute of Nutrition

wantanee.krieng@mahidol.ac.th0-2800-2380

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026