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Application of EIT to determine bladder volume

Not Applicable
Conditions
Healthy volunteerselectrical impedance tomography, non-invasive, urinary bladder volume, ultrasound
Registration Number
DRKS00012871
Lead Sponsor
Klinik für UrologieUniklinik RWTH Aachen
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
10
Inclusion Criteria

Persons who are fully competent and able to understand the nature, significance and scope of the study.
Persons who are able to understand and follow the instructions of the study staff.
Signed consent

Exclusion Criteria

Underage,
Diseases / preoperations of the bladder,
urinary tract infection,
Suffering functional disorder of the bladder,
Renal disease leading to urine production of less than 500ml / 24h or polyuria> 4l / 24h,
Renal insufficiency (GFR <60 ml / min / 1.73 m²),
Ascites, cardiac insufficiency, soft tissue edema, diseases of abdominal water, liver disease,
Metallic implants or electrically active implants (heart pacemakers, defibrillators),
Obesity (BMI> 29),
Diabetes mellitus / insipidus,
Fear of electrical devices (electrophobia),
pregnancy

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Single evaluation of which electrode arrangment is best suited for continuous impedance-based determination of the bladder volume, as well as data collection to evaluate whether accurate knowledge of the body geometry is required for the method.
Secondary Outcome Measures
NameTimeMethod
Furthermore, all safety-relevant data are documented.
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