Clinical Trials Directory

Trials / Completed

CompletedNCT02179112

Determining Universal Processes Related to Best Outcome in Emergency Gastrointestinal Surgery: an International Evaluation

Status
Completed
Phase
Study type
Observational
Enrollment
10,745 (actual)
Sponsor
University of Edinburgh · Academic / Other
Sex
All
Age
Healthy volunteers
Accepted

Summary

A multicentre, international evaluation of emergency abdominal surgery to establish surgical outcomes and identify common, modifiable best practice processes.

Detailed description

Background: With over 200 million surgical operations per year worldwide and with nearly every acute hospital providing surgical services, outcomes from emergency general surgery represent internationally important healthcare markers. Best practice and modifiable processes that are relevant to good patient outcomes around the world require validation using patient-level data. Aim: The primary aim of this study is to identify internationally relevant, modifiable surgical practices (in terms of modifiable equipment and clinical management) associated with best care. These factors will include use of imaging, supplementary oxygen, pulse oximetry, critical care, and safety checklists. Method: This is a multicentre, international, prospective cohort study. Any hospital in the world performing acute surgery will be eligible to enter. Any patient undergoing emergency surgery with an incision entering the peritoneal cavity is eligible. Routine, anonymised clinical data on consecutive patients will be collected over a two week period in each surgical centre, with up to 30 days follow-up data collected. The primary outcome is 24-hour post-operative mortality rate. Secondary outcomes include 30-day inpatient post-operative mortality rate, and 30-day serious complication rate. Participating centres will also be asked to complete a survey that will collect data on hospital structural and resource characteristics. Data will be entered and stored securely via the University of Edinburgh's REDCap system. This pragmatic protocol (which will delivered across many low-resource settings) does not allow for independent verification of data entry. Data collection norms are laid out in the protocol, where data definitions are also clearly provided. Sample size is not relevant to this exploratory audit. Centres will only be included where there is at least 95% data completeness. Potential explanatory variables that will be explored in subsequent analysis include country Human Developmental Index, and resource differences.

Conditions

Interventions

TypeNameDescription
PROCEDUREEmergency Abdominal SurgeryEmergency intra-peritoneal surgery (only exclusion: Caesarian section).

Timeline

Start date
2014-07-01
Primary completion
2017-06-01
Completion
2017-06-01
First posted
2014-07-01
Last updated
2024-05-22

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT02179112. Inclusion in this directory is not an endorsement.