Maestro 1.1 Post-Market Registry | NCT06103136 | Trialant

Maestro 1.1 Post-Market Registry | NCT06103136 | Trialant

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
Patients operated using the Maestro platform			Device: Laparoscopic surgery using the Maestro Platform
Control			Device: Laparoscopic surgery using the Maestro Platform

Interventions

Name	Type	Description	Arm Group Labels	Other Names
Laparoscopic surgery using the Maestro Platform	Device	Patients scheduled for laparoscopic surgery will be operated on as per standard of care, using standard port, surgical table and instrument placements (following local applicable guidelines), and off-the-shelf surgical equipment. Standard of care surgical technique following local applicable guidelines will be used. The Maestro Platform may be used to position and hold the scope as well as the retractor in the locations determined by the surgeon during the procedure, with the ability to revert at any time to standard of care (manual minimally invasive surgery) without the usage of the Maestro Platform, or to convert to open surgery.

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Adverse Events (AEs) in terms of type (device/procedure related), seriousness, level of severity. Rate of occurence of intra-procedural and post-procedural adverse events, and device related complications		Adverse Events (AEs) in terms of type (device/procedure related), seriousness, level of severity. Rate of occurence of intra-procedural and post-procedural adverse events, and device related complications [ Time Frame: 30 days ]
Completion of the procedure using the Maestro Platform without conversion to a manual minimally invasive or open surgical procedure specifically due to a device failure or malfunction		During procedure

Contacts/Locations Module