- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04867499
Epidemiology of Acute Mesenteric Ischemia
March 12, 2022 updated by: Karri Kase, Tartu University Hospital
Retrospective Population-based Study on Epidemiology of Acute Mesenteric Ischemia in Estonia
Retrospective population-based study on epidemiology of acute mesenteric ischemia in Estonia Study objective is to describe epidemiologic features in adult patients with acute mesenteric ischemia during years 2016-2020.
Patients from all hospitals in Estonia are included.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
577
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
-
-
-
Tartu, Estonia
- Tartu University Hospital
-
-
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
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
All at least 18-year-old patients with acute mesenteric ischemia during years 2016-2020 in Estonia.
Description
Inclusion Criteria:
All at least 18-year-old patients with acute mesenteric ischemia during years 2016-2020.
Exclusion Criteria:
-
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Incidence
Time Frame: 2016-2020
|
To identify the incidence of AMI in adult hospitalized patients in Estonia during 2016-2020
|
2016-2020
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
October 5, 2021
Primary Completion (ACTUAL)
February 1, 2022
Study Completion (ACTUAL)
February 1, 2022
Study Registration Dates
First Submitted
April 20, 2021
First Submitted That Met QC Criteria
April 26, 2021
First Posted (ACTUAL)
April 30, 2021
Study Record Updates
Last Update Posted (ACTUAL)
March 15, 2022
Last Update Submitted That Met QC Criteria
March 12, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 21021
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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