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Clinical Trials/NCT06798272
NCT06798272CompletedNot Applicable

Measurement of Skinfold Thickness in Subscapular Area to Monitor Hydration Status in Chronic Hemodialysis Patients

Medical University of Lodz1 site in 1 country50 target enrollmentStarted: October 10, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
50
Locations
1
Primary Endpoint
changes in overhydration

Study Overview

Brief Summary

Background Maintaining fluid balance is one of major challenges of the dialysis therapy. It includes, in particular, the management of "dry body mass". We postulated that simple measurement of subscapular skinfold thickness before and after hemodialysis could help monitor hydration status in chronic dialysis patients.

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •chronic hemodialysis for at least 3 months

Exclusion Criteria

  • •severe mental disabilities, poor compliance, any acute infection, instability of the cardiovascular hemodynamic condition

Arms & Interventions

changes of overhydration during hemodialysis session

Experimental

Intervention: dialysisis with and without glucose in the dialysis (Procedure)

Outcomes

Primary Outcomes

changes in overhydration

Time Frame: From enrollment to one week

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Michal Nowicki

Professor MD

Medical University of Lodz

Study Sites (1)

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