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OpenTrials
Completed

NCT Number: NCT03873701

Bedside Ultrasonography in Acute Patients With Suspected Kidney Involvement

The aim of this study is to evaluate the accuracy and implications of the diagnoses and treatment determined by bedside ultrasonography (b-US) of the kidneys compared to current clinical assessment. Potentially diagnosing patients faster and avoiding missing conditions leading to readmission or unnecessary radiation from computed tomography (CT).

This study evaluates the use of b-US as a supplement to clinical evaluation, in an unselected group of patients in the emergency department (ED) with signs of kidney involvement. The b-US of the kidneys is performed by a medical student certified in this technique. The evaluation will be based on data collected from a Danish hospital (Odense University Hospital, OUH) in autumn 2018.

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Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Suspicion of urinary tract infection and one or more of the following:
  • Flank pain
  • Fever
  • Symptoms when voiding
  • Creatinine elevation or 20% elevation from known creatinine level elevation

Exclusion criteria

  • Age < 18 years
  • Radiological ultrasonographic examination already performed
  • Patients who are not able to consent

Treatment and study plan

bedside ultrasonography

Diagnostic Test

Patients suspicious to urinary tract infection with kidney involvement are being examined by ultrasonography to detect hydroneprhosis. The treating clinicians fill out questionnaires to validate the impact of the bedside ultrasonography on the patient care and treatment.

Other names: Ultrasound

Primary outcomes

  1. Ultrasonographic hydronephrosis

    Time frame: All included patient undergo bedside ultrasonography within 4 hours after admission

    Ultrasonographic hydronephrosis defined by > 1cm pelvic dilation

Secondary outcomes

  1. Clinical consequence of bedside ultrasonographic result

    Time frame: Within 4 hours after admission

    Clinicians responsible for the primary clinical assessment determine treatment and further examinations before and after the ultrasonographic results.

Sponsors and collaborators

Lead sponsor

Odense University Hospital

Other

Collaborators

  • Odense Patient Data Explorative Network

Registry information

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Mar 13, 2019
Registry last updated
Apr 25, 2019

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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