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Clinical Trials in Canada / NCT07242053
Active, not recruiting Not applicable

Margin Intraoperative CT Feedback Feedback Study

NCT07242053 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2024-03-06
Last updated
2026-04-28

Condition(s) studied

Lung Cancer (Diagnosis)

Investigational drug(s) / intervention(s)

Intraoperative CT of resected lung

Intraoperative CT of resected lung: Once the wedge resection is performed, the resected specimen will brought for CT scan

Study summary

To date, there is no established method for confirming whether sufficient margins have been obtained during surgery, only post-surgery by a pathologist. The purpose of this study is to evaluate the impact of intraoperative CT margin feedback on surgical decisions, such as additional removal. The ability to accurately evaluate surgical margins intraoperatively could reduce the risk of locoregional recurrence and eliminate the need for additional treatment after surgery. Moreover, optimal intraoperative feedback to surgeon could influence surgical decision making and contribute to the satisfactory outcome. This is a single center clinical trial. A total of 80 patients scheduled for wedge resections for lung malignancies (including suspected patients) will be enrolled in this study. Nine surgeons in the division of thoracic surgery will also be involved as participants. Once the wedge resection is performed, the resected specimen will be inflated and scanned by CT to measure surgical margin intraoperatively. Surgeons will have access to the CT data and the associated margin data immediately. They then may decide if an additional resection is required. The expected margin surveyed by questionnaire will be compared to CT measured margin, and CT measured margin will be compared to pathological margin questionnaires over course. After the total course of surgery, surgeons will be asked to complete a questionnaire as well to assess the satisfaction by intraoperative feedback.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients scheduled for wedge resection for lung malignancies (included suspected lesions). * 18 years of age or older. Exclusion Criteria: * Any patients with inability to give informed consent * Wedge resection for non-therapeutic purpose, e.g. diagnostic purpose.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
UHN Toronto Ontario

More University Health Network, Toronto trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07242053 on ClinicalTrials.gov ↗ ← All trials in Canada