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Acute Mesenteric IschemiaNCT04867499

Epidemiology of Acute Mesenteric Ischemia

An observational study of Acute Mesenteric Ischemia, run by Tartu University Hospital at 1 site in Estonia.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Acute Mesenteric Ischemia
How many people
577 participants
Where
1 siteEstonia
Study dates
5 Oct 2021to 1 Feb 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: All at least 18-year-old patients with acute mesenteric ischemia during years 2016-2020 in Estonia.

Who may be able to join

  • All at least 18-year-old patients with acute mesenteric ischemia during years 2016-2020.

Who cannot join

  • -

Trial locations and contacts

1 site in 1 country.

Estonia1 site
  • Tartu University Hospital

    Tartu

Other trials in Estonia

About this study

Official title: 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.

Being tested
No intervention

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • No interventionOther

    Descriptive study. No intervention.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Incidence

    To identify the incidence of AMI in adult hospitalized patients in Estonia during 2016-2020

    Measured: 2016-2020

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Apr 2021
  2. Study start5 Oct 2021
  3. Primary completion1 Feb 2022
  4. Study completion1 Feb 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
577 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04867499
Sponsor's protocol ID
21021
Status last verified
Mar 2022
First submitted
20 Apr 2021
Last updated
15 Mar 2022
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Kase K, Reintam Blaser A, Tamme K, Mandul M, Forbes A, Talving P, Murruste M. Epidemiology of Acute Mesenteric Ischemia: A Population-Based Investigation. World J Surg. 2023 Jan;47(1):173-181. doi: 10.1007/s00268-022-06805-5. Epub 2022 Oct 19.

    PubMed 36261602

Questions about this trial

What is this clinical trial studying?

An observational study of Acute Mesenteric Ischemia, run by Tartu University Hospital at 1 site in Estonia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 15 Mar 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Estonia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Incidence (time frame: 2016-2020). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04867499, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Mar 2022.

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