Using cone-beam CT to guide microcoil placement for lung nodules during surgery
Cone-beam Computed Tomography (CT) Guided Microcoil Localization of Pulmonary Nodules During Video Assisted Thoracic Surgery(VATS)
NA · University Health Network, Toronto · NCT02496624
This study is testing if using a special imaging tool during lung surgery can help doctors find and remove lung nodules more accurately and safely.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Health Network, Toronto (other) |
| Locations | 1 site (Toronto, Ontario) |
| Trial ID | NCT02496624 on ClinicalTrials.gov |
What this trial studies
This clinical trial focuses on the use of cone-beam CT technology to accurately localize pulmonary nodules before performing video-assisted thoracic surgery (VATS). The study is conducted by the Guided Therapeutics program at the University Health Network, which integrates advanced imaging and navigational tools to enhance surgical precision. By utilizing a portable intra-operative cone-beam CT, the trial aims to improve the outcomes of lung cancer surgeries through better localization of nodules. The approach is designed to facilitate minimally invasive procedures and potentially reduce complications associated with traditional methods.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older with lung nodules who are suitable for microcoil localization prior to VATS.
Not a fit: Patients who may not benefit from this study include those unable to provide informed consent, those who cannot tolerate general anesthesia, pregnant individuals, and severely obese patients.
Why it matters
Potential benefit: If successful, this approach could lead to more accurate and effective surgical removal of lung nodules, improving patient outcomes in lung cancer treatment.
How similar studies have performed: Other studies utilizing advanced imaging techniques for surgical guidance have shown promising results, indicating potential success for this novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Any adult patient age 18 and older with lung nodules who are candidates for microcoil localization prior to VATS wedge resection Exclusion Criteria: * Patients that are unable to give informed consent * Patients that are unable to tolerate general anesthesia * Patients who are pregnant or patients that believe they are pregnant * Patients with implantable devices susceptible to Radio Frequency (RF) fields * Severely obese patients
Where this trial is running
Toronto, Ontario
- University Health Network — Toronto, Ontario, Canada (RECRUITING)
Study contacts
- Study coordinator: Judy McConnell
- Email: judy.mcconnell@uhn.ca
- Phone: 4165817486
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Lung Cancer