- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02980081
Abdominal Plain X-ray in the Emergency Departement
July 26, 2017 updated by: Olivier T. Rutschmann, University Hospital, Geneva
Abdominal Plain X-ray in the Emergency Departement: Really Usefull?
There are only few recognized indications for the realization of plain abdominal X-rays in the emergency departement.
The objective of this study is to explore the reasons for abdominal plain X-rays prescription in the Emergency departments (EDs) of two hospitals.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
All abdominal plain x-rays prescription will be reviewed in order to identify reasons for prescribing this exam.
The indications will be compared to international guidelines in order to identify whether abdominal plain x-rays are overprescribed.
Reasons for overprescription will be identify by chart review.
Study Type
Observational
Enrollment (Actual)
1997
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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Geneva, Switzerland, 1211
- Geneva University Hospitals, ED
-
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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
16 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
All adult patients during one year in 2 EDs in the state of Geneva, Switzerland, with a prescription of an abdominal plain x-ray
Description
Inclusion Criteria:
- >= 16 years
- prescription of an abdominal plain x-ray during their stay in the ED
Exclusion Criteria:
- < 16 y
- no abdominal plain x-ray prescribed
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 |
Intervention / Treatment |
---|---|
Plain abdominal x-ray
All patients admitted to 2 EDs and with a prescription of an abdominal plain x-ray.
|
Abdominal plain x-ray as prescribed by the emergency physician
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Indications for abdominal plain x-ray prescription
Time Frame: Within 24 hours after ED admission
|
Identification of the indications for abdominal plain x-ray and of the number of patients with appropriate indications accordingly to international guidelines
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Within 24 hours after ED admission
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number and types of other prescribed radiological exams
Time Frame: Within 24 hours after ED admission
|
Describe whether other radiological exams (CT, ultrasonography, MRI) have been performed and their indications.
|
Within 24 hours after ED admission
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Omar Kherad, MD, MPH, Hôpital de La Tour
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
November 1, 2016
Primary Completion (Actual)
June 1, 2017
Study Completion (Actual)
June 1, 2017
Study Registration Dates
First Submitted
November 24, 2016
First Submitted That Met QC Criteria
November 29, 2016
First Posted (Estimate)
December 2, 2016
Study Record Updates
Last Update Posted (Actual)
July 27, 2017
Last Update Submitted That Met QC Criteria
July 26, 2017
Last Verified
July 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CCER 2016-00104
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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