About this trial
This study is designed to evaluate the application of the Maestro Robotic Platform for surgical assistance in laparoscopic abdominal surgery. The purpose of this study is to assess the system use in general surgery on different procedures, level of complexity, and type of setting (elective/emergency).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Aged 18 years or above
Undergoing minimally invasive abdominal surgery
Participant is able to give informed consent for participation in the study.
Disqualifiers
Vulnerable populations
Any medical, psychiatric, or occupational condition, including a history of substance abuse, that may pose additional risk or interfere with study results, as determined by the investigator
Trial population
Patients undergoing laparoscopic abdominal surgery with the assistance of Maestro.
Trial design
Cohort
Prospective
Treatments tested in this trial
Any abdominal laparoscopic surgery with the usage of the Maestro Platform.
Procedure/SurgeryAny abdominal laparoscopic surgery with the usage of the Maestro Platform.
Treatment groups
Trial outcomes
Primary outcomes
Intra-operative outcomes
• All adverse events (description)
Secondary outcomes
Post-operative outcomes- hospitalization
Hospitalization period (days)
Intra-operative measures- complications
Procedure-specific complications (description)
Post-operative outcome- pain
Post-operative pain (pain score 0-4)
Post-operative outcomes- complications
Post-operative complications; descriptions 30 days)
Sponsors and contacts
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