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OpenTrials
Completed

NCT Number: NCT05729126

The Discrepancy in Radiologists' Practice of Intravenous Contrast Imaging Studies Among Chronic Kidney Disease Patients

* There is a discrepancy between protocols used for intravenous imaging for chronic kidney disease including hemodialysis patients among different hospitals and even, among radiologists same selves. * This questionnaire based study aims to quantify that discrepancy and describe the variables associated with the discrepancy.

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Key information

About this study

  • There is a discrepancy between protocols used for intravenous imaging for chronic kidney disease including hemodialysis patients among different hospitals and even, among radiologists same selves.
  • This questionnaire-based study aims to quantify that discrepancy and describe the variables associated with the discrepancy.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Practicing radiologist

Exclusion criteria

  • retired radiologist

Treatment and study plan

questionnare

Other

A questionnaire form is emailed to radiologists to get their response of their practice with hemodialysis and chronic kidney disease patients

Primary outcomes

  1. time from IV contrast study and next dialysis session

    Time frame: 1 day

    time from IV contrast study and next dialysis session

Sponsors and collaborators

Lead sponsor

Benha University

Other

Registry information

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Feb 15, 2023
Registry last updated
Feb 15, 2023

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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