Clinical trial
Post Market Study: Use of the Reusable FloShield 10mm Endoscopic Cannula and Blunt Obturator and the Robotic FloShield System During Robot-assisted Laparoscopic Single-Site Surgery. A Multicenter Historical Control Comparison
NCT02163239 is registered in ClinicalTrials.gov with Minimally Invasive Devices, Inc. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Post Market Study: Use of the Reusable FloShield 10mm Endoscopic Cannula and Blunt Obturator and the Robotic FloShield System During Robot-assisted Laparoscopic Single-Site Surgery. A Multicenter Historical Control Comparison
- Lead sponsor
- Minimally Invasive Devices, Inc.
- Phase
- Observational
- Overall status
- Terminated
- Start date
- March 31, 2015
- Completion date
- September 30, 2015
- Enrollment
- 20 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
benign hysterectomy, cholecystectomy, salingo-oophorectomy