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Central Blood Volume in Hypotensive Dialysis Patients

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: NCT00257504
Recruitment Status : Completed
First Posted : November 23, 2005
Last Update Posted : September 12, 2006
Sponsor:
Information provided by:
Danish State Hospital

Tracking Information
First Submitted Date November 21, 2005
First Posted Date November 23, 2005
Last Update Posted Date September 12, 2006
Study Start Date November 2005
Primary Completion Date Not Provided
Current Primary Outcome Measures Not Provided
Original Primary Outcome Measures Not Provided
Change History
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Central Blood Volume in Hypotensive Dialysis Patients
Official Title Registration of Central Blood Volume in Hypotensive Dialysis Patients - a Comparison of Thoracic Impedance and Central Venous Saturation Monitoring
Brief Summary The purpose of the study is to test whether hypotensive episodes during dialysis - caused by withdrawal of fluid drom the circulation - can be predicted by means of two harmless monitoring techniques.
Detailed Description Not Provided
Study Type Observational
Study Design Observational Model: Case Control
Observational Model: Natural History
Time Perspective: Cross-Sectional
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Not Provided
Study Population Not Provided
Condition Intradialytic Hypotension
Intervention Not Provided
Study Groups/Cohorts Not Provided
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Completed
Enrollment
 (submitted: November¬†21,¬†2005)
20
Original Enrollment Same as current
Study Completion Date May 2006
Primary Completion Date Not Provided
Eligibility Criteria

Inclusion Criteria:

  • Chronic hemodialysis patients with central vascular access

Exclusion Criteria:

  • Patients below 18 years of age
  • Patients unable to give informed consent
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers Not Provided
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Denmark
Removed Location Countries  
 
Administrative Information
NCT Number NCT00257504
Other Study ID Numbers CBV estimation
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Not Provided
Study Sponsor Danish State Hospital
Collaborators Not Provided
Investigators
Study Director: Søren D Ladefoged, MD Danish State Hospital
PRS Account Danish State Hospital
Verification Date September 2006