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Outcome-related Performance Evaluation Through Revision and Analysis of inTraoperative Events

Outcome-related Performance Evaluation Through Revision and Analysis of inTraoperative Events

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06655948
Acronym
OPERATE
Enrollment
700
Registered
2024-10-24
Start date
2024-10-31
Completion date
2029-10-31
Last updated
2024-10-24

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

Conditions

Laparoscopic Abdominal Surgery

Keywords

Intraoperative Adverse Events, Video-Based Assessment, Minimally Invasive Surgery, Surgical Performance, Patient Outcomes

Brief summary

The goal of this prospective, multicentric, observational, cohort study is to evaluate intraoperative adverse events (iAEs) through video-based assessment (VBA) across minimal invasive procedures performed in general surgery departments. The main questions it aims to answer are: * The prevalence, type, and severity of iAEs * Correlation between iAE and clinical outcomes * Correlation between iAE and surgical performance * Qualitative analysis of root cause analysis and mitigation strategies

Detailed description

The OPERATE study is a prospective, multicenter observational cohort study focused on evaluating the prevalence and impact of intraoperative adverse events (iAEs) during minimally invasive surgeries. The study aims to systematically collect and analyze surgical videos and clinical outcomes from multiple centers. By using advanced video-based assessment (VBA) tools, such as the Objective Clinical Human Reliability Analysis (OCHRA) and the Severity of Intraoperative Events and Rectification (SEVERE) index, the study will examine how surgical performance correlates with post-operative outcomes. The study will initially focus on colorectal surgery, with the possibility of expanding to other types of minimally invasive procedures. Videos of the surgeries will be recorded, de-identified, and uploaded to a centralized platform for analysis. The study also seeks to identify root causes of iAEs and develop strategies to prevent them. Data collection will include not only video-based assessments but also patient demographic details, surgical history, and post-operative recovery data. By understanding the frequency and nature of iAEs, this study aims to improve surgical safety, reduce complications, and ultimately enhance the quality of patient care in a broad range of general surgical procedures. The findings may contribute to developing new training protocols, artificial intelligence instruments to model errors and increase procedural safety, and guidelines to optimize surgical performance and patient outcomes.

Interventions

None listed

Sponsors

Fondazione Policlinico Universitario Agostino Gemelli IRCCS
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

* Patients scheduled for elective minimally-invasive surgery in participating centers * Patients with no contraindication to anesthesia and laparoscopic procedures * Capable of providing informed consent

Exclusion criteria

* Surgery performed with palliative intent or under unplanned/emergency setting * Pregnant or breastfeeding patient * Patient under legal custody or guardianship

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of intraoperative adverse eventsDay of the surgical procedure (1 day)The prevalence of iAEs will be assessed using validated VBA tools including the Objective Clinical Human Reliability Analysis (OCHRA), the European Association for Endoscopic Surgery (EAES) classification, and the Severity of Intraoperative Events and Rectification (SEVERE) index.

Secondary

MeasureTime frameDescription
Outcomes correlationFrom the day of the surgical procedure up to 5 years of follow upCorrelation between iAE and clinical outcomes, overall and per iAEs severity
SeverityDay of the surgical procedure (1 day)Prevalence per severity of iAE
Video-Based AssessmentDay of the surgical procedure (1 day)Correlation between iAE and surgical performance assessed through validated VBA tools
Root causesDay of the surgical procedure (1 day)Qualitative analysis of root cause analysis and mitigation strategies

Countries

France, Italy

Contacts

Primary ContactSergio Alfieri, prof
sergio.alfieri@policlinicogemelli.it+390630154477
Backup ContactPietro Mascagni
pietro.mascagni@policlinicogemelli.it

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026