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The effect of cinnamon on the level of FBS and Hb1AC in diabetic patients

comparison of routine drug regime of blood glucose control with cinnamon and routine drug regime with placebo on FBS and Hb1AC in patients with non insulin dependent diabetes; A double blind randomized controlled clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016100230098N1
Enrollment
138
Registered
2016-10-30
Start date
2014-05-22
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

Non-insulin-dependent diabetes. Non-insulin-dependent diabetes mellitus

Interventions

Intervention 1: Intervention group: In addition to routine treatment of diabetes to control blood sugar under approved therapy protocols, patients will receive three500 mg capsules of cinnamon daily b
Treatment - Drugs
Placebo
Intervention group: In addition to routine treatment of diabetes to control blood sugar under approved therapy protocols, patients will receive three500 mg capsules of cinnamon daily before breakfast,
Control group: In addition to routine treatment of diabetes to control blood sugar under approved therapy protocols, samples will receive daily three vitamin C capsules as placebo that their shape, si

Sponsors

Vice chancellor for research, Birjand University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: type II non-insulin dependent diabetes, blood levels of hemoglobin A1C between 6.5 and 7.5, desire to participate in the study. Exclusion criteria: not regular referring to diabetes control center, hemolytic anemia and thalassemia diseases, recent infusion of blood, uremia, allergy to cinnamon, kidney, liver and parathyroid diseases and intestinal problems, pregnancy, lactation, drug intolerance, signs of allergy to cinnamon, taking insulin, unexpected events and death

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Fasting glucose levels. Timepoint: Before intervention and 90 days after taking medication. Method of measurement: Blood sampling and determination of fasting glucose levels by enzymatic method.;Hemoglobin A1C. Timepoint: Before intervention and 90 days after taking medication. Method of measurement: Blood sampling and determination of the glycosylated hemoglobin by HPLC method.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzadeh zahedifar

Birjand University of Medical Sciences

azadehzahedifar@gmail.com+98 28 3322 4609

Outcome results

None listed

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