benign hysterectomy
DeviceRobotic-assisted and laparoscopic hysterectomy for benign disease with the DEXTER robotic surgery system.
NCT Number: NCT07746531
The purpose of this post-market, observational study is to collect real-world data under anticipated conditions of use that demonstrates that the device performs as intended (accurate, precise control of surgical instruments) in patients undergoing robotic-assisted and laparoscopic hysterectomy for benign disease.
Trial opening soon.
Get Notified22 year and older
Female
Observational
Cypress surgery center, Wichita, Kansas, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Robotic-assisted and laparoscopic hysterectomy for benign disease with the DEXTER robotic surgery system.
Time frame: up to 42 days after surgery
Occurrence of Clavien-Dindo grades III-V adverse events
Time frame: Intraoperative
Successful completion of the DEXTER-assisted procedure, i.e. free of any conversion to an open or fully laparoscopic surgical approach
Contact information is provided by the study sponsor or research team.
Distalmotion SA
Industry
ROBOTIC MINIMALLY INVASIVE HYSTERECTOMY POST-MARKET CLINICAL STUDY WITH THE DEXTER ROBOTIC SURGERY SYSTEM
Acronym: MAGENTA
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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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