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OpenTrials
Completed

NCT Number: NCT03096626

Association Between Depression and Iron Metabolism in Hemodialysis Patients

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

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Key information

Conditions

Hemodialysis Behavior Behavioral Symptoms Depression

Sex eligibility

All sexes

Study type

Observational

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. Measurement of depression status

    Time frame: day 1

    Using The Beck Depression Inventory

Secondary outcomes

  1. The values of serum ferritin

    Time frame: day 1

    Measuring serum ferritin levels as iron metabolism

Sponsors and collaborators

Lead sponsor

Yoshihiro Tsuji

Other

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Mar 30, 2017
Registry last updated
Mar 30, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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