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Acute Haemodynamic Effects of Peritoneal Dialysis as Evaluated by Sphygmocor Technology

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00407134
First Posted: December 4, 2006
Last Update Posted: December 28, 2007
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:
University Hospital, Ghent
  Purpose

Subjects with peritoneal dialysis are randomized to different groups. The different groups receive different intra-abdominal volumes and different glucose-concentrations.

The effects on blood pressure and other cardiovascular parameters (e.g. central blood pressure, augmentation index, ...) will be evaluated.


Condition Intervention
Peritoneal Dialysis Procedure: Different abdominal volumes and different glucose-concentrations during peritoneal dialysis

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Acute Haemodynamic Effects of Peritoneal Dialysis as Evaluated by Sphygmocor Technology

Further study details as provided by University Hospital, Ghent:

Primary Outcome Measures:
  • Blood pressure

Estimated Enrollment: 20
Study Start Date: December 2006
Study Completion Date: April 2007
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Subjects with peritoneal dialysis
  • Aged 18-80 years
  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): NCT00407134


Locations
Belgium
University Hospital Ghent
Ghent, Belgium, 9000
Sponsors and Collaborators
University Hospital, Ghent
Investigators
Principal Investigator: Wim Van Biesen, MD, PhD University Hospital, Ghent
  More Information

Additional Information:
ClinicalTrials.gov Identifier: NCT00407134     History of Changes
Other Study ID Numbers: 2006/382
First Submitted: November 30, 2006
First Posted: December 4, 2006
Last Update Posted: December 28, 2007
Last Verified: December 2007