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ProSat - Effect of Probiotics on Satiety

Probiotics and Satiety - Acute Effects and Persistence of Acute Effects

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00826761
Acronym
ProSat
Enrollment
22
Registered
2009-01-22
Start date
2009-01-31
Completion date
Unknown
Last updated
2012-06-15

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

Conditions

Appetite Regulation, Obesity

Brief summary

The aim of the ProSat study is to examine the effects of a probiotic capsule containing one of two doses (low and high dose) of Lb. Casei on subjective appetite sensation, ad libitum energy intake, and appetite hormone response in a single meal test and to determine whether the acute effects persist after daily supplementation of the probiotic capsule.

Interventions

DIETARY_SUPPLEMENTprobiotic

One capsule per meal test (high dose or low dose)

DIETARY_SUPPLEMENTplacebo

1 capsuel every morning

Sponsors

Chr Hansen
CollaboratorINDUSTRY
University of Copenhagen
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
20 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy men and women * Normal to slight overweight (BMI: 22-28 kg/m2) * 20-45 years of age

Exclusion criteria

* Smoking * Daily medicine use (oral contraceptives excluded) * Use of pre- and probiotic supplements and foods * Blood donation 3 months prior to the study * Hb\<8mmol/l * Chronic illnesses such as hyperlipidemia, diabetes inflammatory diseases * Pregnancy or breastfeeding * Elite athletes (\>10 hours hard exercise/week) * Vegetarians

Design outcomes

Primary

MeasureTime frame
Glucose; Insulin; GLP-1; CCK; PYY; grehlin; PP; amylin; LPS; TNF-alfa; hsCRP; fibrinogen2013

Secondary

MeasureTime frame
Subjective appetite measurements; Spontaneous food intake2012

Countries

Denmark

Outcome results

None listed

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