Use of da Vinci system for thoracic surgery
What is the Purpose of this Study?
If you choose to join this study, we will use the da Vinci SP® Surgical System during your procedure. We will collect information related to your procedure from your medical records and phone calls with you. This information will collected before your surgery and for up 30 days after. If you are being treated for cancer, this information will be collected for up to 5 years.
What is the Condition Being Studied?
Pulmonary Lobectomy (removal of Part of Lung) and Thymectomy (Removal of Thymus) Procedures
Who Can Participate in this Study?
Adults who have surgery planned or scheduled to remove part of the lung or thymus gland.
For more information about who can join this study, please contact the study team at kathleen.lane@duke.edu.
Age Group
Adults
Participating Institutions
What is Involved?
We are doing this to learn more about the safety and performance of the da Vinci SP® Surgical System in pulmonary lobectomy and thymectomy procedures.
Study Details
Full Title
A Prospective, Multi-Center Investigation of the da Vinci SP® Surgical System in Pulmonary Lobectomy and Thymectomy for Benign and Malignant Disease
Principal Investigator
Contacts
Kathleen Lane
Email: kathleen.lane@duke.edu
Protocol Number
IRB:
PRO00109932
NCT:
NCT05150210
ClinicalTrials.gov
View on ClinicalTrials.gov