We're building a better ClinicalTrials.gov. Check it out and tell us what you think!
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Postprandial Hemodynamics

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.
 
ClinicalTrials.gov Identifier: NCT01027507
Recruitment Status : Completed
First Posted : December 8, 2009
Last Update Posted : December 8, 2009
Sponsor:
Information provided by:
Skane University Hospital

Brief Summary:
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 or disease
Heart Disease

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.

Layout table for study information
Study Type : Observational
Actual Enrollment : 23 participants
Observational Model: Case-Only
Official Title: Relationship Between Postprandial Alterations in Hemodynamics, Blood Pressure, Blood Glucose, Insulin Concentrations, Gastric Emptying, and Satiety
Study Start Date : January 2009
Actual Study Completion Date : November 2009




Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
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

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
Layout table for location information
Sweden
Departments of Medicine, Malmö University Hospital
Malmö, Sweden, 205 02
Sponsors and Collaborators
Skane University Hospital
Investigators
Layout table for investigator information
Principal Investigator: Joanna Hlebowicz, MD, PhD Skane University Hospital
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Layout table for additonal information
Responsible Party: Lars Stavenow, Departments of Medicine, Malmö University Hospital
ClinicalTrials.gov Identifier: NCT01027507    
Other Study ID Numbers: 353/2008b
First Posted: December 8, 2009    Key Record Dates
Last Update Posted: December 8, 2009
Last Verified: December 2009
Additional relevant MeSH terms:
Layout table for MeSH terms
Heart Diseases
Cardiovascular Diseases