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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02821923
Other study ID # Poly Vasc
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 7, 2016
Est. completion date March 10, 2022

Study information

Verified date May 2022
Source University Hospital, Basel, Switzerland
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Sugar alcohols such as xylitol and erythritol are increasingly popular as sugar substitutes in the food industry and are also recommended to diabetic patients. Both substances are already in use in the food industry and are freely available. Since the 1970s, beneficial effects on oral health could be demonstrated as oral bacteria were influenced positively. A pilot study recently undertaken in the US (Flint N, 2014) has shown that diabetics profit from a daily intake of erythritol, as this natural sweetener enhances the elasticity of the blood vessels. In this trial, investigators aim to examine whether this effect can be found in a non-diabetic but obese cohort, and whether also xylitol improves vascular function.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date March 10, 2022
Est. primary completion date March 10, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria: - Obese volunteers (BMI > 30kg/m2) - Aged 18- max. 55 years - Otherwise healthy. Exclusion Criteria: - Known cardiovascular disease - Diabetes mellitus - Smoking and drug abuse - Arterial hypertension with antihypertensive treatment - Dyslipidaemia with statin therapy - Known chronic hepatic disease (NASH, hepatitis). - Known renal disease: kidney failure - Pregnancy - Chronical diseases of the gastrointestinal tract, history of gastrointestinal surgery with major changes to the gastrointestinal tract - Substance abuse, alcohol abuse. - Inability to follow procedures due to psychological disorders, dementia or insufficient knowledge of project language (German).

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
E967-Xylitol
24g xylitol/d
E968-Erythritol
36g erythritol/d

Locations

Country Name City State
Switzerland University Hospital Basel

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Central arterial stiffness measured by sonography Change from baseline to 5 weeks after intake of polyol
Secondary Glucose tolerance measured by oral glucose tolerance test Change from baseline to 5 weeks after intake of polyol
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