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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
November 30, 2006
December 4, 2006
December 28, 2007
December 2006
Not Provided
Blood pressure
Same as current
Complete list of historical versions of study NCT00407134 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
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Acute Haemodynamic Effects of Peritoneal Dialysis as Evaluated by Sphygmocor Technology
Acute Haemodynamic Effects of Peritoneal Dialysis as Evaluated by Sphygmocor Technology

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.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Peritoneal Dialysis
Procedure: Different abdominal volumes and different glucose-concentrations during peritoneal dialysis
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
20
April 2007
Not Provided

Inclusion Criteria:

  • Subjects with peritoneal dialysis
  • Aged 18-80 years
Sexes Eligible for Study: All
18 Years to 80 Years   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Belgium
 
 
NCT00407134
2006/382
No
Not Provided
Not Provided
Not Provided
University Hospital, Ghent
Not Provided
Principal Investigator: Wim Van Biesen, MD, PhD University Hospital, Ghent
University Hospital, Ghent
December 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP