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The Effects of Crocin Supplementation on Metabolic Parameters, Oxidative Stress, AMP- Activated Protein Kinase and Inflammation-promoting Genes Expression in Peripheral Blood Mononuclear Cells in Patients With Type 2 Diabetes

N

National Nutrition and Food Technology Institute

Status

Completed

Conditions

Type 2 Diabetes

Treatments

Dietary Supplement: placebo
Dietary Supplement: crocin

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

To study the effects of crocin supplement in patients with type 2 diabetes, 50 patients will be randomly allocated to placebo group and 2 tablets of crocin for 12 weeks. At the first and the end of the intervention, lipid profiles, blood pressure, blood sugar, inflammatory and anthropometric factors will be assessed and compared between groups.

Enrollment

50 patients

Sex

All

Ages

40 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age of 40 to 65 years type 2 diabetes: and body mass index range of 18.5 to 30 kg/m2

Exclusion criteria

pregnancy or lactation A history of Cardiovascular disease, Pulmonary disease, Renal disease

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

50 participants in 2 patient groups, including a placebo group

placebo
Placebo Comparator group
Treatment:
Dietary Supplement: placebo
crocin
Active Comparator group
Treatment:
Dietary Supplement: crocin

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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