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Thermogenic Effect of Ginger

Double-blind Placebo-controlled Clinical Trial of Thermogenic Effect of Ginger (Zingiber Officinale) in Eutrophic Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03089593
Enrollment
20
Registered
2017-03-24
Start date
2017-03-27
Completion date
2017-06-14
Last updated
2017-06-21

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

Conditions

Healthy Volunteers

Keywords

Thermic Effect of Food, Energy Expenditure, Ginger

Brief summary

The main objective of the study is to evaluate the thermogenic effect of ginger.

Detailed description

Healthy and eutrophic women will receive capsules of 200 mg of ginger extract (5% active ingredient) or placebo (cellulose), along with a standardized breakfast, with a minimum seven days washout period.

Interventions

The volunteers will receive two capsules containing 200mg of extract of ginger with 5% of gingerols (20 mg). Breakfast will be offered (bread, butter, turkey ham and industrialized fruit juice) and the participants will have 15 minutes to eat it.

The volunteers will receive two capsules containing cellulose (placebo). Breakfast will be offered (bread, butter, turkey ham and industrialized fruit juice) and the participants will have 15 minutes to eat it.

Sponsors

Federal University of Minas Gerais
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Females; * Aged between 18 and 60 years old; * Body mass index between 18.5 and 24.9 kg/m²; * Agree to sign the informed consent.

Exclusion criteria

* Any chronic health conditions (e.g. diabetes, hypertension, chronic renal failure, heart and liver disease); * Previous operation for weight loss; * Medications known to affect total energy expenditure; * Pregnancy and breast-feeding; * Smoking; * Alcohol use (\>2 doses/day).

Design outcomes

Primary

MeasureTime frameDescription
Change in postprandial energy expenditureBaseline and thereafter at 30, 60, 120, 180 and 240 minutes postprandialEnergy expenditure will be assessed by indirect calorimetry

Secondary

MeasureTime frameDescription
Change in oxygen consumptionBaseline and thereafter at 30, 60, 120, 180 and 240 minutes postprandialOxygen consumption will be assessed by indirect calorimetry
Change in blood pressureBaseline and thereafter at 30, 60, 120, 180 and 240 minutes postprandialBlood pressure will be assessed using digital sphygmomanometer
Change in axillary temperatureBaseline and thereafter at 30, 60, 120, 180 and 240 minutes postprandialAxillary temperature will be assessed using a digital thermometer
Change in metabolic profileBaseline and thereafter at 30, 60, 120 and 240 minutes postprandialTotal cholesterol
Change in heart rateBaseline and thereafter at 30, 60, 120, 180 and 240 minutes postprandialHeart rate will be assessed using digital sphygmomanometer

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026