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
ConditionsRenal Insufficiency, Chronic
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
Investigators
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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