Clinical Trials Directory

Trials / Unknown

UnknownNCT01103167

Body Composition Monitor in Hemodialysis Patients

The Association Between Body Composition and Biomarkers in Hemodialysis Patients

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
160 (estimated)
Sponsor
Gachon University Gil Medical Center · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Control of volume status is a pivotal issue in haemodialysis therapy. Objective and practical management for maintaining normovolemia is needed. The investigators hypothesized that intervention of volume status with the body composition monitor (BCM) may improved hemodynamic parameters and biomarkers in hemodialysis patients.

Detailed description

The investigators will assess BCM in enrolled hemodialysis patients by 4 weeks for 16 weeks During the former 8-week intervention period, The investigators will adjust patients' volume status according to the results of BCM. During the latter 8-week observational period, The investigators will evaluate the changes of patients' hemodynamic parameters and biomarkers.

Conditions

Interventions

TypeNameDescription
BEHAVIORALcontrol of ultrafiltrationDuring the interventional period, dry weight of patients will be adjusted according to the results of body composition.

Timeline

Start date
2010-04-01
Primary completion
2010-10-01
Completion
2010-12-01
First posted
2010-04-14
Last updated
2010-04-14

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01103167. Inclusion in this directory is not an endorsement.