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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03025997
Other study ID # NL59245.068.16
Secondary ID 163042
Status Completed
Phase N/A
First received January 6, 2017
Last updated November 16, 2017
Start date January 24, 2017
Est. completion date March 31, 2017

Study information

Verified date March 2017
Source Maastricht University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluates the ability of encapsulation of orally applied lipids in a yoghurt snack to modify ad libitum food intake and satiety, without GI symptoms. Every subject receives two treatments (active, and placebo) on two different days, following a randomized cross-over design.


Recruitment information / eligibility

Status Completed
Enrollment 33
Est. completion date March 31, 2017
Est. primary completion date March 31, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- BMI between 25-30 kg/m2

- Voluntary participation

Exclusion Criteria:

- Milk (-protein or lactose)- allergy/intolerance

- History of serious GI complaints/surgeries

- Pregnancy, lactation

- Excessive alcohol consumption (>20 per week)

- Abnormal eating behaviour

- Intention to stop smoking

- Reported unexplained weight loss or gain in the month prior to screening

- Self-admitted HIV-positive state

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Active yoghurt
Active yoghurt (containing encapsulated lipid) will be ingested after a standardized breakfast, and subsequently satiety and food intake will be measured.
Placebo yoghurt
Placebo yoghurt (containing non-encapsulated lipid) will be ingested after a standardized breakfast, and subsequently satiety and food intake will be measured.

Locations

Country Name City State
Netherlands Maastricht University Maastricht

Sponsors (2)

Lead Sponsor Collaborator
Maastricht University Medical Center Wageningen University and Research Centre

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary ad libitum food intake t=0: standardized breakfast, t=90 minutes: yoghurt, t=210 minutes: ad libitum food intake 2 hours after yoghurt snack
Secondary Satiety feelings Every 15-30 min, 5 attributes will be measured on a Visual Analogue Scale Up to 3.5 hours on each of the 2 test days.
Secondary occurrence and severity of GI symptoms Every 15-30 min, 4 attributes will be measured on a Visual Analogue Scale Up to 3.5 hours on each of the 2 test days.
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