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Clinical Trial Summary

To confirm the safety and performance of the da Vinci SP Surgical System, Instruments and Accessories in pulmonary lobectomy, and in thymectomy procedures.


Clinical Trial Description

Primary performance: The primary endpoint will be assessed as the ability to complete the planned da Vinci SP-assisted thoracic procedure without conversion to an alternate approach. Conversion to an alternate approach comprises undocking of the da Vinci SP to complete the planned procedures using other methods, such as open, VATS, or multiport robotic (da Vinci SI or X/Xi) Primary Safety: The primary safety endpoint will be assessed as the incidence of all intra-operative and post-operative adverse events that occur through the 30-day follow-up period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05150210
Study type Interventional
Source Intuitive Surgical
Contact
Status Active, not recruiting
Phase N/A
Start date July 20, 2022
Completion date July 2028

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