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Fizzy Drinks Study

C

Clinical Nutrition Research Centre, Singapore

Status

Completed

Conditions

Satiety
Gastric Emptying
Glycemic Response

Treatments

Other: High carbonation
Other: No Carbonation
Other: Low carbonation

Study type

Interventional

Funder types

Other

Identifiers

NCT02735889
2015/01079

Details and patient eligibility

About

The objective of this study is to compare the effect of different levels of carbonation isocaloric beverages on glycemic response (using protocol based on standardized glycemic index testing methodology), gastric emptying and satiety. It is hypothesized that carbon dioxide will delay gastric emptying, and in turn, attenuate glycemic response and enhance satiety. The use of a non-nutrient (gas) in improving glycemic response and satiety would have important health implications for the beverage industry.

Full description

15-20 healthy subjects will be recruited for the study by means of advertisements, flyers and personal communications.

A randomized, cross-over design experiment with three treatments will be carried out. Three different beverages will be prepared:- No carbonation (NC): Potable water + sugar- Low carbonation (LC): Potable water + sugar + little CO2- High carbonation (HC): Potable water + sugar+ high CO2.

The outcome measures assessed will be glycemic response, gastric emptying and satiety. Glycemic response will be measured by taking capillary blood samples (<5ul) by fingerpricking with one-time use sterilized lancets. Gastric emptying will be assessed by ultrasonography methodology developed by Okabe et al, 2015. Satiety will be measured using electronic visual analogue scales assessing hunger, fullness, desire to eat, prospective consumption and thirst. In addition, participants will be asked to rate the level of effervescence of beverage, sweetness of beverage, amount of beverage consumed, as well as how pleasant the beverage was immediately after drinking of test beverage. Feelings of bloatedness will be assessed using electronic visual analogue scales administered at 0, 15, 30, 45, 60, 90,120 min from drinking of test beverage. At the end of the test session, ad libitum lunch will be served, and the amount of food and drinks consumed will be measured (by weight difference before and after serving).

Enrollment

15 patients

Sex

All

Ages

21 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy adult
  • Aged between 21 - 40 years old
  • BMI between 18.0-30.0 kg/m2
  • Blood pressure < 140/80 mmHg
  • Fasting blood glucose < 6.0mmol/L
  • Fasting blood glucose < 6.0mmol/L

Exclusion criteria

  • Are a smoker
  • Have symptoms or medical history of gastrointestinal, cardiovascular, diabetes, cancer or other illnesses/diseases/conditions that could affect gastric motility and appetite
  • Are on prescription medication
  • Had a major medical or surgical event requiring hospitalization within the preceding 3 months.
  • Are taking part in other clinical trials concurrently
  • Are taking part in sports at competitive/endurance levels
  • Have a score equal or greater than 3.7 for restrained eating in Dutch Eating Behaviour Questionnaire.
  • Have special dietary requirements or food allergies.

Trial design

15 participants in 3 patient groups

No carbonation (control)
Other group
Description:
No carbonation (NC, control): Potable water + sugar
Treatment:
Other: No Carbonation
Low carbonation
Active Comparator group
Description:
Low carbonation (LC): Potable water + sugar + little CO2
Treatment:
Other: Low carbonation
High carbonation
Active Comparator group
Description:
High carbonation (HC): Potable water + sugar+ high CO2
Treatment:
Other: High carbonation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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