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Rapid Versus Slow Ingestion of Mixed Meal: Influence on Islet and Incretin Hormone Secretion in Healthy Volunteers

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01779622
First Posted: January 30, 2013
Last Update Posted: September 30, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Bo Ahren, Lund University
  Purpose
To test the influence of rapid versus slow ingestion of a mixed meal on insulin and incretin hormone secretion in healthy volunteers

Condition Intervention
Healthy Volunteers Recruited From the General Population Other: Mixed meal

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Basic Science
Official Title: Rapid Versus Slow Ingestion of Mixed Meal: Influence on Islet and Incretin

Further study details as provided by Bo Ahren, Lund University:

Primary Outcome Measures:
  • Area under the curve for insulin [ Time Frame: 300 min ]

Secondary Outcome Measures:
  • Area under the curve for glucose-dependent insuinotropic polypeptide [ Time Frame: 300 min ]
  • Area under the curve for glucagon-like peptide-1 [ Time Frame: 300 min ]

Other Outcome Measures:
  • Area under the curve for glucagon [ Time Frame: 300 min ]

Enrollment: 24
Study Start Date: June 2013
Study Completion Date: June 2014
Primary Completion Date: January 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: 1
Healthy volunteers are ingesting a mixed meal either rapidly or slowly
Other: Mixed meal
Ingestion of mixed meal

Detailed Description:
A mixed meal (524 kcal) is ingested rapidly (within 5 min) or slowly (10-15 min) and changes in insulin, glucagon, GIP and GLP-1 levels are followed for subsequent 300 min
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Healthy subjects

Exclusion Criteria:

  • Diabetes Liver disease Kidney disease Thyroid disease
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01779622


Locations
Sweden
Department of Clinical Sciences, Lund University
Lund, Sweden, 22184
Sponsors and Collaborators
Lund University
  More Information

Additional Information:
Responsible Party: Bo Ahren, Professor, Lund University
ClinicalTrials.gov Identifier: NCT01779622     History of Changes
Other Study ID Numbers: 17
2013-000449-38 ( EudraCT Number )
First Submitted: January 27, 2013
First Posted: January 30, 2013
Last Update Posted: September 30, 2014
Last Verified: September 2014

Keywords provided by Bo Ahren, Lund University:
mixed meal¨
insulin
glucagon
GIP
GLP-1

Additional relevant MeSH terms:
Incretins
Hormones
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs