Small Bowel Obstruction. A Prospective Multicener Study
SBO
A Multicenter Prospective Study on Small Bowel Obstruction
1 other identifier
observational
214
1 country
1
Brief Summary
To get an overview of patients hospitalized with mechanical small bowel obstruction and the evaluate the use of contrast media as part of conservative management. To analyze how many patients were operated on and in how many cases conservative measures helped.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2021
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
October 15, 2022
CompletedFirst Submitted
Initial submission to the registry
December 4, 2022
CompletedFirst Posted
Study publicly available on registry
December 22, 2022
CompletedDecember 6, 2023
November 1, 2023
12 months
December 4, 2022
November 29, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Resolution on SBO
Resolution of small bowel obstruction (passing gas/flatus, contrast media in the colon on the X-ray )
Hospitalization period (approximately 5 days)
Study Arms (1)
Patients hospitalized with small bowel obstruction
Patients hospitalized with a certain diagnosis during a certain period of time
Interventions
Observational study, no intervention
Eligibility Criteria
Patients hospitalized with mechanical small bowel obstruction
You may qualify if:
- aged 18 years or older with mechanical small bowel obstruction who signed an informed consent form
You may not qualify if:
- Patients younger than 18 years, patients with large bowel obstruction or dynamic small bowel obstruction and/or patients who had undergone abdominal/pelvic surgery within 4 weeks of admission were excluded from the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Tartulead
- North Estonian Medical Centercollaborator
Study Sites (1)
Tartu University Hospital
Tartu, Tartu, 50406, Estonia
Study Officials
- PRINCIPAL INVESTIGATOR
Liis Jaanimäe
University of Tartu
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- General Surgeon, PhD student
Study Record Dates
First Submitted
December 4, 2022
First Posted
December 22, 2022
Study Start
May 1, 2021
Primary Completion
April 30, 2022
Study Completion
October 15, 2022
Last Updated
December 6, 2023
Record last verified: 2023-11