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The effect of resitant dextrin prebiotic on type 2 diabetes

The effect of resitant dextrin prebiotic( nutriose FM06) supplementation on IL4, IL12 and metabolic endotoxima in the patients with type 2 diabetes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015020520965N1
Enrollment
80
Registered
2015-02-23
Start date
2015-03-19
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Type 2 diabetes. Endocrine, Nutritional and metabolic diseases

Interventions

Intervention 1: Placebo group will receive 10 gram of maltodextrin powder in the form of 5 gram packs with breakfast and dinner meals for 8 weeks. The supplement will be given monthly and during the
Placebo
Treatment - Drugs
Placebo group will receive 10 gram of maltodextrin powder in the form of 5 gram packs with breakfast and dinner meals for 8 weeks. The supplement will be given monthly and during the consumption pos
Resistant dextrin group will receive 10 gram of Resistant dextrin powder in the form of 5 gram packs with breakfast and dinner meals for 8 weeks. The supplement will be given monthly and during the

Sponsors

Tabriz University Of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age 30-50 years old; 25= BMI <35; having diabetes at least 6 months prior to the study; consumption of blood glucose lowering drug; ?ber intake <25 g ?ber/day. Exclusion criteria: Consumption of antioxidants supplements during last 3 months; using insulin, pregnancy; lactation; acute renal disease.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
IL4. Timepoint: Before and after 8 weeks of intervention. Method of measurement: ELISA.;IL12. Timepoint: Before and after 8 weeks of intervention. Method of measurement: ELISA.;LPS. Timepoint: Before and after 8 weeks of intervention. Method of measurement: ELISA.

Secondary

MeasureTime frame
BMI. Timepoint: At baseline and after 8 weeks of intervention. Method of measurement: Weight divided by Height Square.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParvin Dehghan

Tabriz University Of Medical Sciences

dehghan.nut@gmail.com00

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026