Post Market Study for FloShield 10mm Reusable Cannula and Blunt Obturator and Robotic FloShield
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
Sponsor: Minimally Invasive Devices, Inc.
Terminated
Not meeting primary objective of the study
Listed as NCT02163239, this observational or N/A phase trial focuses on Benign Hysterectomy and Cholecystectomy and remains terminated or withdrawn. Sponsored by Minimally Invasive Devices, Inc., it has been updated 7 times since 2015, reflecting limited change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.
Status Flow
Change History
7 versions recorded-
Sep 2024 — Present [monthly]
Terminated
-
Jul 2024 — Sep 2024 [monthly]
Terminated
-
Jan 2021 — Jul 2024 [monthly]
Terminated
-
Jun 2018 — Jan 2021 [monthly]
Terminated
-
Apr 2018 — Jun 2018 [monthly]
Terminated
Phase: NA → None
▶ Show 2 earlier versions
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Feb 2017 — Apr 2018 [monthly]
Terminated NA
-
Jan 2017 — Feb 2017 [monthly]
Terminated NA
First recorded
Mar 2015
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Minimally Invasive Devices, Inc.
For direct contact, visit the study record on ClinicalTrials.gov .