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Mechanism of Action of Vichy Catalan Water

Mechanism of Action of Vichy Catalan Water

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01334840
Enrollment
21
Registered
2011-04-13
Start date
2009-11-30
Completion date
2010-07-31
Last updated
2014-07-30

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

Conditions

Cardiovascular Diseases

Keywords

Cardiovascular risk, Cholecystokinin, Gallbladder emptying, Lipid absorption, Postprandial triacylglycerols, Sodium-bicarbonated mineral water

Brief summary

Water consumption is essential to maintain hydration and good health. Sodium-bicarbonated mineral waters are reported to have beneficial digestive and hypocholesterolemic properties. The aim of this study was to investigate the effects of the consumption of a sodium-bicarbonated mineral water (BW) with or without a meal, compared to a low mineral content water as a control water (CW), on postprandial serum triacylglycerols (TAG), cholecystokinin (CCK), and gallbladder volume.

Interventions

DIETARY_SUPPLEMENTBicarbonated mineral water

Volunteers fasted overnight consumed: 0.5 L of the bicarbonated mineral water without meal or, 0.5 L of the bicarbonated mineral water with meal

DIETARY_SUPPLEMENTMineral water low in mineral content (control)

Volunteers fasted overnight consumed: 0.5 L of the control water without meal or, 0.5 L of the control water with meal

Sponsors

Vichy Catalán, Spain
CollaboratorUNKNOWN
National Research Council, Spain
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Adult (\>18 and \<40 years) * BMI \>18 and \<30 kg/m2

Exclusion criteria

* Age \<18 and \> 40 years * TAG \> 250 mg/dL (2.82 mmol/L) * Being a usual consumer of carbonic mineral water * Obesity * Diabetes * Hypertension or digestive, liver and renal disease * Biliary obstruction * Eating disorders * Being under medication that could affect lipid metabolism * Consumption of functional foods that could affect lipid metabolism (food containing n-3 fatty acids or phytosterols)

Design outcomes

Primary

MeasureTime frame
Serum triacylglycerolsBaseline

Secondary

MeasureTime frame
Serum glucoseBaseline
Serum insulinBaseline
CholecystokininBaseline
Gallbladder volumeBaseline
AldosteroneBaseline

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026