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Effects of Capsimax on Appetite, Energy Intake and Blood Pressure

Effects of Capsimax on Appetite, Energy Intake and Blood Pressure

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04874701
Enrollment
63
Registered
2021-05-06
Start date
2018-01-07
Completion date
2019-07-02
Last updated
2021-05-06

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

Conditions

Obesity, Body Weight, Weight Loss, Overweight

Brief summary

Obesity is an ongoing major public health problem in most countries of the world for which the agrifood industry still remains criticized because of the abundant offer of high sugar-lipid-energy dense foods, particularly in the fast-food sector. The resulting societal pressure on the food industry probably explains in part the efforts that have been deployed to seek natural active ingredients and to develop functional foods favorably influencing energy balance. Capsaicin is a food non-nutrient constituent that was shown to decrease appetite sensations and subsequent energy intake. The measurement of heart rate variability revealed an association between the increase in sympathetic nervous system (SNS) activity and the satiating effects induced by capsaicin. This is concordant with the observation that pre-prandial intake of capsaicin, be it in capsules or diluted in tomato juice, increased satiety and reduced energy intake. The objective of this study is to evaluate the long effects of Capsimax on appetite sensations and energy expenditure under conditions of moderate energy restriction and to evaluate the long-term effects of Capsimax on energy intake and expenditure under conditions of moderate energy restriction.

Interventions

Capsimax, 2 capsules per day, for 12 weeks Medicinal ingredient: Capsicum annuum Quantity (per capsule): 100.0 mg

Personalised diet plan targeting a 500 kcal/day energy restriction

Sponsors

OmniActive Health Technologies
CollaboratorINDUSTRY
Laval University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Premenopausal women * Between 18 and 50 years * Healthy * Non-smoker * BMI between 25 and 35 kg/m2 * Weight stability

Exclusion criteria

* Pregnant or menopausal woman * History of losing and gaining weight (yo-yo) * Taking medication for diabetes, hypertension, depression, or hypothyroid * Taking a supplement for weight loss * Vegetarian, vegan, intolerant to gluten or pepper (investigational product), and severe allergy to peanuts or nuts * Suffers from Irritable Bowel Syndrome or gastro-oesophageal reflux * Suffers from stomach ulcers or inflammation * Other serious conditions such as cardiovascular, renal, liver, and lung diseases * History of drug abuse and current alcohol abuse * Use of any medication (including over-the-counter medications and herbal remedies) such as grapefruit juice, piperine, NSAIDs, etc.

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in appetite sensations, energy intake and food preferences at Week 1212 weeksVisual analog scales used after a standardized breakfast and a buffet-type meal to measure hunger, fullness, satiety and desire to eat.
Change from Baseline in energy expenditure at Week 1212 weeksEnergy expenditure measured at fasting stade, after a 15 minutes rest, by indirect calorimetry
Change from Baseline in Body weight and fat at Week 1212 weeksBody weight and fat measured with Dual-energy X-ray absorptiometry (DXA)
Change from Baseline in Blood pressure at Week 1212 weeksBlood pressure measured every 30 minutes during a 3h testing

Secondary

MeasureTime frameDescription
Change from Baseline Microbiota analysis at Week 1212 weeksSequencing of the 16S DNA to evaluate the evolution of the microbiota according to the diet.
Change from Baseline anxiety (BDI and STAI) at Week 1212 weeksThe State-Trait Anxiety Inventory (STAI) is a commonly used measure of trait and state anxiety. It can be used in clinical settings to diagnose anxiety and to distinguish it from depressive syndromes. The Beck Depression Inventory (BDI) is a 21-item, self-report rating inventory that measures characteristic attitudes and symptoms of depression.
Change from Baseline System analysis of endocannabinoids at Week 1212 weeksThe evaluation of the endocannabinoid system done on OpenArray TaqMan according to the expression in RNA of about fifty genes of this system and by their quantification by HPLC coupled to MS / MS mass spectrometry and / or by ion capture. IT-TOF
Change from Baseline sleeping quality (PSQI) at Week 1212 weeksThe Pittsburgh Sleep Quality Index (PSQI) is a validated questionnaire which evaluates sleep quality and disturbance over a 1-month time interval. The PSQI gives a score for seven different components : subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping. medication, and daytime dysfunction
Change from Baseline Feeding behaviors (TFEQ and Food cravings questionnaire) at Weeks 1212 weeksFeeding behaviors measured by two validated questionnaires : The Three Factor Eating Questionnaire (TFEQ) which measures three main dimensions of human eating behaviors such as cognitive restraint, disinhibition and susceptibility for hunger and the Food cravings questionnaire

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026