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ACUTE-Acute Surgical Care- Risk Factors and Outcomes for Patients in Need of Acute Surgical Care

ACUTE-Acute Surgical Care- Risk Factors and Outcomes for Patients in Need of Acute Surgical Care

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05195697
Acronym
ACUTE
Enrollment
3000
Registered
2022-01-19
Start date
2020-01-01
Completion date
2030-12-01
Last updated
2026-06-17

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

Conditions

Complication of Anesthesia, Complication of Surgical Procedure, Complication of Treatment, Long Term Effects After Emergency Surgery, Long Term Effects After GI Bleeding, Risk Factors

Keywords

Emergency surgery, Acute surgery, Complications, Risk factors, Frailty, Ageing

Brief summary

Observational retrospective study of patients in need of acute surgical care admitted to Skåne University Hospital between 2009 and 2019.

Detailed description

At Skåne University Hospital approximately 6000 individuals are treated for acute abdominal diseases each year. Given the high number of patients, there is an urgent need to optimize acute surgical care. Lower complication rates would decrease hospital stay, health care costs as well as personal suffering. Assessment instruments for risks and frailty are not validated for the acute setting and the investigators hypothesize there is room for improvement in prophylactic interventions and risk assessment. The investigators will study cohorts of patients with three different surgical diagnosis: acute pancreatitis, gastrointestinal bleeding and perforated ulcer aiming to identify risk factors for complications or death and to investigate assessment tools in this population. Using propensity score analysis, the investigators will try to identify treatment options associated with better outcome for subcohorts defined by frailty, comorbidity, age or gender. Specific factors of interest include: time to- and kind of treatment, handling of ongoing pharmacological therapy (anticoagulants, corticosteroids) and need for further treatments on a long time basis. The results from this project will be used in a future prospective study where prophylactic treatments and specific treatment options are studied.

Interventions

OTHERObservational study of different treatments and time to treatment

Different treatment based on the clinical decision

Sponsors

Region Skane
Lead SponsorOTHER
Lund University
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

Patients admitted to Skåne University hospital in need of acute surgical care -

Exclusion criteria

Below 18 years old \-

Design outcomes

Primary

MeasureTime frameDescription
Mortality5 yearsDefined by Swedish registers
Reintervention5 yearsDefined by medical records
Recurrent disease5 yearsDefined by medical records

Secondary

MeasureTime frameDescription
Lengths of hospital stay5 yearsdefined by medical records
Number of interventions5 yearsdefined by medical records
complications5 yearsdefined by medical records and Swedish Registers

Countries

Sweden

Contacts

CONTACTSara Regnér, PhD
sara.regner@med.lu.se040 33 10 00
CONTACTJenny Eckner, PhD
jenny.eckner@skane.se040 33 10 00
PRINCIPAL_INVESTIGATORSara Regnér, PhD

Region Skane

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 18, 2026