Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
589 participants
OBSERVATIONAL
2020-11-03
2022-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Study population
All patients undergoing emergency abdominal surgery for infection or occlusion and treated with bowel resection with or without anastomosis; intestinal bypass or adhesiolysis
Application of ERAS protocol
Application of a standardized ERAS protocol for the perioperative perioperative management of patients undergoing emergency surgery
Interventions
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Application of ERAS protocol
Application of a standardized ERAS protocol for the perioperative perioperative management of patients undergoing emergency surgery
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* emergency surgery for post-operative complications of post diagnostic procedures
18 Years
ALL
No
Sponsors
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University of Milano Bicocca
OTHER
Responsible Party
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Principal Investigators
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Marco Braga, MD
Role: PRINCIPAL_INVESTIGATOR
University of Milano Bicocca
Locations
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Ospedale Manzoni
Lecco, LC, Italy
ASST Monza
Monza, MB, Italy
Ospedale San Raffaele
Milan, Mi, Italy
ASST Lodi
Lodi, , Italy
Azienda ospedaliero-universitaria Pisana,Ospedale Cisanello
Pisa, , Italy
Ospedale San Jacopo
Pistoia, , Italy
Policlinico Gemelli
Roma, , Italy
Ospedale di Cattinara
Trieste, , Italy
Countries
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Other Identifiers
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ERAS in CDU
Identifier Type: -
Identifier Source: org_study_id
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