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Clinical Trials/NCT00397306
NCT00397306
Completed
Not Applicable

Study for the Evaluation of a Bioimpedance Method for Determination of Dry Weight in Dialysis Patients

University Hospital, Saarland1 site in 1 country16 target enrollmentNovember 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Renal Insufficiency, Chronic
Sponsor
University Hospital, Saarland
Enrollment
16
Locations
1
Primary Endpoint
Bioimpedance Dry weight
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

The purpose of this study is the evaluation of a bioimpedance method for determination of dry weight in dialysis patients. Additionally normal tissue hydration in non-Dialysis patients is investigated in healthy subjects and patients with chronic kidney disease in stages K/DIGO I-IV

Registry
clinicaltrials.gov
Start Date
November 2006
End Date
September 2008
Last Updated
17 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
University Hospital, Saarland

Eligibility Criteria

Inclusion Criteria

  • clinically stable on dialysis within the last three months
  • signed written informed consent

Exclusion Criteria

  • acute myocardial infarction or stroke within the last six months
  • heart failure stage NYHA IV
  • concommitant participation in other interventional trials
  • psychiatric conditions that prevent subject from following the study procedures / protocol
  • pregnancy or lactation
  • limb amputation
  • cardiac pacemaker
  • joint implants
  • implantable pumps and other metallic implants
  • For healthy subjects and CKD patients in stages K/DIGO I-IV the above mentioned criteria other than the first mentioned are applicable respectively.

Outcomes

Primary Outcomes

Bioimpedance Dry weight

Secondary Outcomes

  • Resistivity
  • Blood pressure
  • Wall thickness LA, LV
  • Resistance
  • LV Diameter
  • Shortening Fraction
  • EPO-Dose
  • Quality of Life

Study Sites (1)

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