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Postprandial Hemodynamics

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01027507
First Posted: December 8, 2009
Last Update Posted: December 8, 2009
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:
Skane University Hospital
  Purpose
To study the postprandial alterations in hemodynamics and blood pressure in relation to gastric emptying rate, postprandial blood glucose, plasma concentrations of insulin, satiety in healthy subjects.

Condition
Heart Disease

Study Type: Observational
Study Design: Observational Model: Case-Only
Official Title: Relationship Between Postprandial Alterations in Hemodynamics, Blood Pressure, Blood Glucose, Insulin Concentrations, Gastric Emptying, and Satiety

Further study details as provided by Skane University Hospital:

Enrollment: 23
Study Start Date: January 2009
Study Completion Date: November 2009
Detailed Description:
Ingestion of a meal increase blood flow to the gastrointestinal organs and affects the heart rate, blood pressure, and cardiac output. It is not known through wich mechanisms the heart function changes affects after a meal.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Healthy subjects without symptoms or a history of gastrointestinal disease, abdominal surgery or diabetes mellitus, were included in this crossover study.
Criteria

Inclusion Criteria:

  • Healthy subjects

Exclusion Criteria:

  • history of gastrointestinal disease, abdominal surgery or diabetes mellitus
  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): NCT01027507


Locations
Sweden
Departments of Medicine, Malmö University Hospital
Malmö, Sweden, 205 02
Sponsors and Collaborators
Skane University Hospital
Investigators
Principal Investigator: Joanna Hlebowicz, MD, PhD Skane University Hospital
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Lars Stavenow, Departments of Medicine, Malmö University Hospital
ClinicalTrials.gov Identifier: NCT01027507     History of Changes
Other Study ID Numbers: 353/2008b
First Submitted: December 7, 2009
First Posted: December 8, 2009
Last Update Posted: December 8, 2009
Last Verified: December 2009

Additional relevant MeSH terms:
Heart Diseases
Cardiovascular Diseases