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A Danish Audit of Small Bowel Obstruction

A Danish Audit of Small Bowel Obstruction

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04750811
Acronym
DASBO
Enrollment
540
Registered
2021-02-11
Start date
2021-02-22
Completion date
2026-03-01
Last updated
2024-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bowel Obstruction Small

Keywords

Small Bowel Obstruction

Brief summary

Small bowel obstruction (SBO) is a common and potentially life-threatening acute surgical condition. A minority of patients present with a clear indication for urgent surgical intervention, either on the basis of clinical or radiological assessment (clinical signs of peritonitis/sepsis; suspicion of bowel ischaemia; closed loop obstructions; irreducible herniae etc.). However, the optimal management of the remaining patients, the majority of whom present with SBO caused by abdominal adhesions, remains a topic of international debate with practice varying in different healthcare systems. This multicentre, prospective, observational study aims to describe the current management of patients admitted with SBO in 6 acute hospitals (Bispebjerg, Herlev, Hillerød, Hvidovre, Køge, Slagelse) on the island of Sjælland, Denmark, which accounts for a 1/3 of the total Danish population.

Detailed description

This is a prospective, non-interventional observational study of the management and outcomes of patients admitted with SBO in Denmark. Relevant clinicopathological demographics will be retrieved from consenting patients' medical records. An initial analysis will be performed once these patients have reached 90 days follow-up after the start of treatment. The long-term outcomes of treatment will be assessed with further analyses at 1, 3 and 5 years follow-up.

Interventions

None listed

Sponsors

Danish Small Bowel Obstruction Collaborative
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years old * Radiological or clinical diagnosis of mechanical SBO * Admitted to one of the 6 participating centres

Exclusion criteria

* SBO presenting within 30 days of a previous abdominal operation

Design outcomes

Primary

MeasureTime frame
30-day mortality rate30 days
30-day morbidity rate30 days

Secondary

MeasureTime frame
To describe the proportion of patients undergoing operative versus non-operative managementFrom 90 days
To determine the success rate of non-operative management in patients with SBO and identify predictors of success/failureFrom the start of treatment until 90-days follow-up
To determine the incidence and consequence of malnourishment in patients with SBO90 days
To determine the incidence and consequence of acute kidney injury in patients with SBO90 days
90-day mortality rate90 days

Other

MeasureTime frame
To determine the incidence of recurrent SBO at 1-year, 3-year and 5-year follow-up.Up to 5 years

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026