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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03096626
Other study ID # Uhyogo2
Secondary ID
Status Completed
Phase N/A
First received March 24, 2017
Last updated March 29, 2017
Start date December 1, 2016
Est. completion date March 1, 2017

Study information

Verified date March 2017
Source University of Hyogo
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study assesses the association of depression symptoms and iron metabolism in patients undergoing hemodialysis.


Description:

The Beck Depression Inventory (BDI), second version, was used to quantify the levels of depression. Mean age, duration of HD, hemoglobin levels, serum ferritin levels, serum iron levels, TSAT, TIBC, serum albumin levels, CRP and energy consumption (kcal/week) were included in the model as multivariate variables. Backward stepwise logistic regression (ROC) analysis was performed.


Recruitment information / eligibility

Status Completed
Enrollment 152
Est. completion date March 1, 2017
Est. primary completion date March 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients with stable undergoing hemodialysis

Exclusion Criteria:

- Patients those who refused to join present study, and those who could not complete the questionnaires by themselves, and the patients with chronic hepatitis B or C were excluded.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Yoshihiro Tsuji

Outcome

Type Measure Description Time frame Safety issue
Primary Measurement of depression status Using The Beck Depression Inventory day 1
Secondary The values of serum ferritin Measuring serum ferritin levels as iron metabolism day 1
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