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

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

      • Geneva, Switzerland, 1211
        • Geneva University Hospitals, ED

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
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.

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

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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