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OpenTrials
Completed

NCT Number: NCT04648644

Application of ERAS Protocol in Emergency Surgery

This study defines a standardized protocol inspired to the ERAS philosophy for the peri-operative treatment of patients undergoing emergency abdominal surgery. Primary endpoint is the feasibility of the application of the standardized protocol; secondary endpoint is the safety

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Ospedale Manzoni, Lecco, LC, Italy

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients undergoing emergency abdominal surgery for abdominal sepsis or occlusion and treated with bowel resection with or without anastomosis, intestinal bypass or adhesiolysis.

Exclusion criteria

  • age <18
  • emergency surgery for post-operative complications of post diagnostic procedures

Treatment and study plan

Application of ERAS protocol

Other

Application of a standardized ERAS protocol for the perioperative perioperative management of patients undergoing emergency surgery

Primary outcomes

  1. Feasibility: % of application of post-operative ERAS items

    Time frame: 30 days

    Compliance to the standardize protocol for each item

Secondary outcomes

  1. Safety: complications rate within 30 days

    Time frame: 30 days

    Complication rate and mortality

Sponsors and collaborators

Lead sponsor

University of Milano Bicocca

Other

Registry information

Acronym: ERAS in CDU

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Dec 1, 2020
Registry last updated
Jul 28, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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