- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03074084
Acute Abdomen in Adults- a Prospective Study on Emergency Department Admissions
March 5, 2020 updated by: Tampere University Hospital
Acute Abdomen in Adults- a Prospective Study on Causes of Abdominal Pain Leading to Emergency Department Admission in Tampere University Hospital
This is a non-randomized, prospective, population-based, single-center study designed to evaluate conditions resulting emergency admission in patients with abdominal pain.
Furthermore, we are interested in how many patients are discharged with "non-specific abdominal pain" but later readmitted and diagnosed with a specific diagnosis.
Study Overview
Status
Recruiting
Conditions
Detailed Description
1000 adult patients with acute abdominal pain will be recruited at Tampere University Hospital Emergency department.
The patients will fill in a questionaire about the symptoms and their duration.
A urine sample will be collected for polyamine molecule analysis with an electronic nose.
At later stage of the study, a serum sample for coeliac tests will be collected.
Patient outcome will be obtained during the hospital stay, at one-month after discharge and at one year.
Study Type
Observational
Enrollment (Anticipated)
1000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Mika T Ukkonen, MD, PhD, MEcon
- Phone Number: +358443454523
- Email: mika.ukkonen@fimnet.fi
Study Contact Backup
- Name: Leena M Saaristo, MD
- Phone Number: +358405030201
- Email: leena.saaristo@fimnet.fi
Study Locations
-
-
-
Tampere, Finland
- Recruiting
- Tampere University Hospital
-
Contact:
- Satu-Liisa K Pauniaho, MD, PhD
- Phone Number: +358505386783
- Email: satu-liisa.pauniaho@pshp.fi
-
Contact:
- Mika T Ukkonen, MD, PhD, MEcon
- Phone Number: +358443454523
- Email: mika.ukkonen@fimnet.fi
-
-
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
the adult patients with abdominal pain admitted to the emergency department are included.
One thousand patients from Tampere district will be chosen for analysis.
Description
Inclusion Criteria:
All adult patients with abdominal pain.
Exclusion Criteria:
Under the age of 18 years
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 |
---|---|---|
Number of patients with specific diagnose
Time Frame: One month
|
Population based analysis of incidence of diseases
|
One month
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Number of patients misdiagnosed in emergency department and requiring readmission
Time Frame: One month
|
One month
|
Number of participants with treatment related adverse events
Time Frame: One month
|
One month
|
Diagnostic accuracy of polyamine molecule analysis
Time Frame: One month
|
One month
|
Number of patients with undiagnosed coeliac disease
Time Frame: One month
|
One month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Satu-Liisa K Pauniaho, MD, PhD, Tampere University Hospital, Finland
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
June 1, 2016
Primary Completion (Anticipated)
December 1, 2021
Study Completion (Anticipated)
December 31, 2025
Study Registration Dates
First Submitted
October 20, 2016
First Submitted That Met QC Criteria
March 3, 2017
First Posted (Actual)
March 8, 2017
Study Record Updates
Last Update Posted (Actual)
March 6, 2020
Last Update Submitted That Met QC Criteria
March 5, 2020
Last Verified
March 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R16006
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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