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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03275948
Other study ID # 2016/487
Secondary ID
Status Completed
Phase N/A
First received September 6, 2017
Last updated October 2, 2017
Start date November 1, 2016
Est. completion date October 2, 2017

Study information

Verified date October 2017
Source Lund University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to investigate, in healthy middle age subjects, effects of whole grain rye on cognitive functions, mood, and cardiovasculair risk markers


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date October 2, 2017
Est. primary completion date February 28, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years to 70 Years
Eligibility Inclusion Criteria:

- healthy

- BMI 19-28

- plasma glucose < 6.1 mmol/L

- non smooker

Exclusion Criteria:

- known metabolic diseases

- known gastrointestinal disorders

- known cognitive decline.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
whole grain
whole grain rye
reference
white wheat bread

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Lund University

Outcome

Type Measure Description Time frame Safety issue
Primary cognitive performance test of working memory capacity postprandial 0-180 min after breakfast
Secondary glucose tolerance postprandial glucose concentrations 0-180 min after breakfast