OTTAVA Robotic System
DeviceProcedure with the OTTAVA Robotic System
NCT Number: NCT06709261
This study assesses safety and performance of the OTTAVA Robotic System, through 30 days postoperative, in subjects undergoing robotic-assisted Roux-en-Y Gastric Bypass (RYGB) procedure.
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Notify Me21 year and older
All sexes
Interventional
Not applicable
Orlando Health, Orlando, Florida, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Criteria for Inclusion:
Criteria for Exclusion:
Procedure with the OTTAVA Robotic System
Time frame: Procedure day
Time frame: Through 30 days post-procedure
Time frame: Through 30 days post-procedure
Time frame: Procedure day
Time frame: Procedure day
Time frame: Procedure day
Time frame: Procedure day
Time frame: Hospital stay, assessed up to 30 days
Time frame: Through 30 days
Time frame: Through 30 days
Time frame: Through 30 days
Time frame: Through 30 days
Time frame: Through 30 days
Auris Health, Inc.
Industry
EDS-2022-01: Safety and Performance of the OTTAVA™ Robotic System: A Prospective, Multi-Center Evaluation (FORTE)
Acronym: FORTE
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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