Monitoring of Hydration Status in Chronic Hemodialysis Patients
NCT ID: NCT06798272
Last Updated: 2025-01-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
50 participants
INTERVENTIONAL
2021-10-10
2024-03-15
Brief Summary
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Aim of the study The aim of the study was to compare the conventional methods of monitoring hydration status during hemodialysis with an assessment of skin fold thickness.
Materials and Methods 50 participants (21 F, 29 M; age 60 ±15 years) were enrolled. Directly before the hemodialysis session the following parameters were measured: body composition with bioimpedance spectroscopy, skinfold thickness in subscapular area with standardized caliper and blood tests: blood count, urea, n-terminal pro B-type natriuretic peptide (nt-proBNP) and pro-adrenomedullin (pro-ADM). The procedures were repeated at the end of three consecutive hemodialysis sessions.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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changes of overhydration during hemodialysis session
dialysisis with and without glucose in the dialysis
there were assessed three consecutive hemodialysis sessions
Interventions
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dialysisis with and without glucose in the dialysis
there were assessed three consecutive hemodialysis sessions
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Medical University of Lodz
OTHER
Responsible Party
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Michal Nowicki
Professor MD
Locations
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Central University Hospital
Lodz, , Poland
Countries
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Other Identifiers
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163/20
Identifier Type: -
Identifier Source: org_study_id
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