- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06805149
Evaluation of Emergency Computed Tomography in Suspected Renal Colic. This is an Observational Retrospective Study Aimed to Evaluate Emergency Computed Tomography in Patients at the Emergency Department in Helsingborg, Sweden, With Suspected Acute Renal Colic.
September 9, 2025 updated by: Region Skane
Evaluation of Emergency Computed Tomography in Suspected Renal Colic
The goal of this observational study is to learn more about diagnostics in patients with suspected acute renal colic at the emergency department. The main questions it aims to answer are:
- How many patients with symtoms of urolithiasis have a stone in the urinary tract at the emergency computed tomography (CT)
- Location and size of the stones.
- Evaluate time to intervention and closure and if this has changed due to emergency CT.
Participants are patients with symtoms of suspected acute renal colic at the emergency department in Helsingborg with an emergency CT within 24 hours.
Study Overview
Status
Completed
Conditions
Detailed Description
Since October 2022 The National Guidelines in Sweden recommend emergency CT for patients with suspected acute renal colic at the emergency department.
In May 2023 the Department of Urology implemented this new regime with emergency CT for these patients in collaboration with the Department of Emergency and the Department of Radiology.
This study aims to evaluate the first year (May 2023 to May 2024) with this new regime.
Data regarding these patients where gathered regarding decriptive data, data regarding the stone, interventions and follow up.
The investigators aim to compare the data with data from a soon to be published (Scandinavian Journal of Urology) article evaluating the situation regarding these patients during one year 2018-2019.
Study Type
Observational
Enrollment (Actual)
1500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Helsingborg, Sweden
- Urology Department
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients at the emergency department in Helsingborg
Description
Inclusion Criteria:
- Patient at the emergency department with suspected acute renal colic and an emergency CT within 24 hours 10 May 2023 to 9 May 2024.
Exclusion Criteria:
- None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Emergency CT: kidney stone?
Patients at the emergency department in Helsingborg with suspected acute renal colic with an CT within 24 hours.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numbers of patients with a kidney stone on emergency CT
Time Frame: From enrollment until the date participants are considered stone free, up to 6 months regarding participants with stone. For participants without a stone, the time frame extends over the duration of their hospitalization, up to 30 days.
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Number of patients with a kidney stone on emergency CT.
Size and location of the stone as well as time to intervention and closure for those with a stone.
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From enrollment until the date participants are considered stone free, up to 6 months regarding participants with stone. For participants without a stone, the time frame extends over the duration of their hospitalization, up to 30 days.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numbers of visits to the emergency department
Time Frame: Time from enrollment until the date the participants are considered stone free, up to 6 months.
|
Has the number of visits to the emergency department due to acute renal colic changed before and after implementation of emergencty CT
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Time from enrollment until the date the participants are considered stone free, up to 6 months.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Magnus Wagenius, Senior consultant, PhD, Urology Department Helsingborg
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 9, 2023
Primary Completion (Actual)
January 1, 2025
Study Completion (Actual)
May 1, 2025
Study Registration Dates
First Submitted
January 15, 2025
First Submitted That Met QC Criteria
January 27, 2025
First Posted (Actual)
February 3, 2025
Study Record Updates
Last Update Posted (Estimated)
September 16, 2025
Last Update Submitted That Met QC Criteria
September 9, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Neurologic Manifestations
- Male Urogenital Diseases
- Calculi
- Pathological Conditions, Anatomical
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Urolithiasis
- Nephrolithiasis
- Pathological Conditions, Signs and Symptoms
- Signs and Symptoms
- Urogenital Diseases
- Pain
- Kidney Calculi
- Urologic Diseases
- Kidney Diseases
- Urinary Calculi
- Renal Colic
Other Study ID Numbers
- 2024-01345-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
We have no plans to share participants data outside the research group at the moment.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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