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NCT Number: NCT06655948

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

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

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

IHU Strasbourg, Strasbourg, France

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About this study

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.

Who can participate

Healthy volunteers accepted: No

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

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

Treatment and study plan

Primary outcomes

  1. Prevalence of intraoperative adverse events

    Time frame: Day 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 outcomes

  1. Outcomes correlation

    Time frame: From the day of the surgical procedure up to 5 years of follow up

    Correlation between iAE and clinical outcomes, overall and per iAEs severity

  2. Severity

    Time frame: Day of the surgical procedure (1 day)

    Prevalence per severity of iAE

  3. Video-Based Assessment

    Time frame: Day of the surgical procedure (1 day)

    Correlation between iAE and surgical performance assessed through validated VBA tools

  4. Root causes

    Time frame: Day of the surgical procedure (1 day)

    Qualitative analysis of root cause analysis and mitigation strategies

Study contacts

Contact information is provided by the study sponsor or research team.

Pietro Mascagni

CONTACT

[email protected]

Sergio Alfieri, prof

CONTACT

[email protected]

+390630154477

Sponsors and collaborators

Lead sponsor

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Other

Registry information

Acronym: OPERATE

Important dates

Study start
2024
Primary completion
2027
Study completion
2029
First posted
Oct 24, 2024
Registry last updated
Oct 24, 2024

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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