- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04455087
Analysis of Complementary Exams Prescriptions From an Emergency Unit of a University Hospital (CEinED)
June 29, 2020 updated by: Pr. Semir Nouira, University of Monastir
Complementary Exams in Emergency Department
The objective of this study is to evaluate the appropriateness of prescribing additional tests in the emergency unit of the University Hospital of Monastir.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The objective of this study is to evaluate the appropriateness of prescribing additional tests in the emergency unit of the University Hospital of Monastir.
Study Type
Observational
Enrollment (Actual)
2000
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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Monastir, Tunisia, 5000
- Hospital of Fattouma Bourguiba
-
-
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
1 year and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
all patients consulting urences of Monastir aged more than 1 year
Description
Inclusion Criteria:
- all patients consulting Emergency Department of Monastir aged more than 1 year
Exclusion Criteria:
- age < 1 year
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 |
---|---|
before intervention
1000 patients befor sensitization
|
sensitization of doctor to decrease the prescription of abuse exams
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
The analysis focused on the appropriateness or otherwise of the complementary exams
Time Frame: The analysis focused on the appropriateness or otherwise of the complementary exams
|
The analysis focused on the appropriateness or otherwise of the complementary exams
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: semir nouira, phd, Netherlands: Ministry of Health, Welfare and Sports
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
April 1, 2013
Primary Completion (Actual)
January 1, 2017
Study Completion (Actual)
February 1, 2017
Study Registration Dates
First Submitted
April 8, 2014
First Submitted That Met QC Criteria
June 29, 2020
First Posted (Actual)
July 2, 2020
Study Record Updates
Last Update Posted (Actual)
July 2, 2020
Last Update Submitted That Met QC Criteria
June 29, 2020
Last Verified
June 1, 2020
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- complementary exams
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
not yet
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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