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CompletedNCT05145673Updated Dec 6, 2021

Effect of Aqueous Cinnamon Extract on the Postprandial Glycaemia Levels in Type 2 Diabetes Mellitus

An interventional study of Placebo (OGTT) and Cinnamon (OGTT plus aqueous cinnamon extract) in Type 2 Diabetes, sponsored by Egas Moniz - Cooperativa de Ensino Superior, CRL. Completed. Open to participants aged 35 Years to 77 Years. Per ClinicalTrials.gov, last updated 2021-12-06.

Sponsored by Egas Moniz - Cooperativa de Ensino Superior, CRL · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 5 years 9 months after the study started (first participant enrolled Jan 2016, registered Nov 2021).
Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
35 Years to 77 Years
Sex
All
01

Study summary

The type 2 diabetes mellitus is a chronic disease and it is a highly prevalent globally. Cinnamon is a spicy used on the traditional cuisine, which have as been associated with beneficial effects on postprandial blood glucose levels (BGL). The aim of the present study was to investigate the effect of cinnamon tea (6g C. burmannii/100mL) on postprandial glycaemia in type 2 diabetic adults.

Following ethical committee approval, thirty-six subjects were selected and randomly allocated in 2 groups (n=18): cinnamon group, which was administrated OGTT (oral glucose tolerance test) followed by cinnamon tea; control group, which was administrated only OGTT. At baseline, anthropometric data, medical condition and pharmacological therapy were collected. A 24-hour dietary recall was taken preceding each intervention. Food Processor SQL (version 10.5.9) program was used to analyze the food nutritional composition. Chemical analysis was performed for total phenols determinations (adapted from Prabha et al) and antioxidant activity for FRAP and for DPPH tests (adapted from K. Thaipong et al.) Statistical analysis was performed using SPSS Statistics program. Data are mean±SEM.

Read the detailed description

Type 2 diabetes mellitus (DM2) subjects aged between 35-77 years were recruited into this study through nutrition appointment, Holon Pharmacy from Lisbon and Portalegre, Portugal. After the approval of the Ethics Committee, 36 individuals, were selected and invited to participate in this study. After eligibility criteria applied, a randomized controlled clinical trial, blind to participants, was conducted to 36 DM2 subjects. Participants were randomly assigned to intervention (n=18) or control group (n=18). The first participant of the study was randomly allocated to intervention or control group and the following participants were systematically allocated in each group. The anonymity and the confidentiality of the participants data collected were guaranteed through a code attributed to each participant. The control group was given a glucose solution to oral glucose tolerance test (OGTT) and the intervention group was given a glucose solution to OGTT followed by a cinnamon aqueous extract. The glucose solution consist in a glucose drink with 75g of anhydrous D-Glucose dissolved in 200 mL of water at room temperature, as prescribed by ADA. The blood glucose levels were measured before intervention at fasting (t0) and after 30 (t30), 60 (t60, 90 (t90) and 120 (t120) minutes after intervention from both groups.

Aqueous cinnamon extract was prepared by Cinnamomum burmannii bark (from Sucrame Company, Portugal) with Indonesia origin. Sticks of cinnamon (60 g) were soaked into 1000 mL of water. After 24 h at room temperature, cinnamon solution was heated for 30 min at 100°C and then filtered at room temperature. After the cinnamon tea preparation a 100 mL individual dose was distributed to each participant. For chemical analysis, a hydromethanolic extract (50 : 50) was performed with aqueous cinnamon extract previously obtained.

Anthropometric paraments and pharmacological therapy data were collected at the beginning of the study. At day before the intervention, a 24-hour food recall questionnaire was employed to participants of the study and carefully instructed by an investigator to complete the food record. The Food Processor SQL (10.14.2. version) programme was applied to analysed the nutritional composition of meals, such as, total energy intake (Kcal), proteins (g), lipids (g), carbohydrates (g), dietary fibre (g) and soluble fibre (g). It were also estimated the glycemic index and glycemic load of food intake.

Based on the blood glucose values, the blood glucose incremental area under the curve (AUCi) of each participant was defined using the GraphPad Prism program (version 5.0). Maximum concentrations (Cmax) and variations of maximum concentrations (ΔCmax) were determined by comparing with its respective baseline glycemia levels values.

The total phenolic concentration in the C. burmanni extract was determined according to Folin-Ciocalteu method employing gallic acid as standard. For the determination of antioxidant activity two methods were performed: FRAP and DPPH, adapted by Thaipong et al. The FRAP method for determination of ferric reducing effect was based on the reduction, at low pH, employing a colourless ferric complex (Fe3+) to a blue-coloured ferrous complex (Fe2+) by electron-donating antioxidants action in 2,4,6-tri(2-pyridyl)-s-triazine (TPTZ) presence.

02

Conditions studied

03

In context

Diabetes Mellitus

10,925 studies on the registry are indexed under Diabetes Mellitus; 1,318 are open to participants now.

This study's enrollment of 36 is below the median of 80 across 8,367 interventional studies indexed under Diabetes Mellitus.

Browse Diabetes Mellitus studies →

Lead sponsor

Egas Moniz - Cooperativa de Ensino Superior, CRL is the lead sponsor of 40 studies on the registry; 21 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
35 Years to 77 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • subjects aged 18 years or older
  • subjects with DM2 diagnostic and men or non-pregnant women.

Exclusion criteria

Exclusion Criteria:

  • insulin-treated subjects
  • history of gastrointestinal symptoms/diseases
  • allergy to cinnamon
  • fasting less than 8 hours
  • cinnamon intake at day before the intervention
  • intense exercise until 2 hours before the intervention
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
36 participants (actual)

Study arms

  • Placebo comparator
    Placebo (OGTT)

    The control group was given an glucose solution to oral glucose tolerance test (OGTT) .

    Other: Placebo (OGTT)

  • Experimental
    Cinnamon (OGTT plus aqueous cinnamon extract)

    The Experimental group was given an glucose solution to oral glucose tolerance test (OGTT) followed by aqueous cinnamon extract.

    Other: Cinnamon (OGTT plus aqueous cinnamon extract)

Interventions

  • OtherPlacebo (OGTT)

    The control group was given an glucose solution to oral glucose tolerance test (OGTT) The glucose solution consist in a glucose drink with 75g of anhydrous D-Glucose dissolved in 200 mL of water at room temperature, as prescribed by ADA. The blood glucose levels were measured before intervention at fasting (t0) and after 30 (t30), 60 (t60, 90 (t90) and 120 (t120) minutes after intervention from both groups.

  • OtherCinnamon (OGTT plus aqueous cinnamon extract)

    The intervention group was given an glucose solution to OGTT followed by a cinnamon aqueous extract. The glucose solution consist in a glucose drink with 75g of anhydrous D-Glucose dissolved in 200 mL of water at room temperature, as prescribed by ADA. The blood glucose levels were measured before intervention at fasting (t0) and after 30 (t30), 60 (t60, 90 (t90) and 120 (t120) minutes after intervention from both groups.

06

What researchers measure

Primary outcomes

  1. Blood glucose levels at beginning

    Mean values of blood glucose levels from both control and experimental groups

    Time frame: At beginning (before intervention)

  2. Blood glucose levels at 30 minutes

    Mean values of blood glucose levels from both control and experimental groups

    Time frame: At 30 minutes after intervention

  3. Blood glucose levels at 60 minutes

    Mean values of blood glucose levels from both control and experimental groups

    Time frame: At 60 minutes after intervention

  4. Blood glucose levels at 90 minutes

    Mean values of blood glucose levels from both control and experimental groups

    Time frame: At 90 minutes after intervention

  5. Blood glucose levels at 120 minutes

    Mean values of blood glucose levels from both control and experimental groups

    Time frame: At 120 minutes after intervention

  6. Incremental area under the curve of blood glucose

    Based on the blood glucose values, the blood glucose incremental area under the curve (AUCi) of each participant was defined using the GraphPad Prism program (version 5.0)

    Time frame: At 120 minutes after intervention

  7. Variation of blood glucose maximum concentration

    Mean values of glucose maximum concentration variation

    Time frame: At 60 minutes after intervention

Secondary outcomes

  1. Anthropometric parameters - body weight

    Mean values of body weight (in kilogram - Kg)

    Time frame: At baseline

  2. Anthropometric parameters - height

    Mean values of Height (in centimeters - cm)

    Time frame: At baseline

  3. Anthropometric parameters - waist circumference

    Mean values of waist circumference (in centimeters - cm)

    Time frame: At baseline

  4. Anthropometric parameters - body mass index

    Mean values of body mass index (Kg/m2), calculated as weight (Kg) divided by height (m2) squared (Kg/m2)

    Time frame: At baseline

  5. Anthropometric parameters - Skeletal muscle mass

    Mean values of Skeletal muscle mass (in kilogram - Kg)

    Time frame: At baseline

  6. Anthropometric parameters - visceral fat

    Mean values of visceral fat (cm3)

    Time frame: At baseline

  7. Pharmacological therapy

    Percentage of antidiabetic orals (biguanide, sulfonylurea, alpha-glucosidase inhibitor, dipeptidyl peptidase 4 inhibitors

    Time frame: At baseline

  8. Total protein intake

    Means values of total protein intake (in grams - g) obtained through The Food Processor SQL software

    Time frame: At baseline

  9. Total lipid intake

    Means values of total lipid intake (in grams - g) obtained through The Food Processor SQL software

    Time frame: At baseline

  10. Total carbohydrate intake

    Means values of total carbohydrate intake (in grams - g) obtained through The Food Processor SQL software

    Time frame: At baseline

  11. Total energy intake

    Means values of total energy intake (in kilocalorie - Kcal) obtained through The Food Processor SQL software

    Time frame: At baseline

  12. Total polyphenols content

    Mean values of total polyphenols content of cinnamon extract (mg/L equivalent of gallic acid)

    Time frame: At baseline

  13. Antioxidant activity

    Mean values of antioxidant activity of cinnamon extract by FRAP and DPPH assays (micromol Trolox/L)

    Time frame: At baseline

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 6, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05145673
Lead sponsor
Egas Moniz - Cooperativa de Ensino Superior, CRL
Responsible party
Sponsor
First posted
Dec 6, 2021
Start date
Jan 19, 2016
Primary completion
Oct 3, 2016
Completion
Oct 31, 2016
Last update
Dec 6, 2021

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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