# Post Market Study for FloShield 10mm Reusable Cannula and Blunt Obturator and Robotic FloShield

> **NCT02163239** · — · TERMINATED · sponsor: **Minimally Invasive Devices, Inc.** · enrollment: 20 (actual)

## Conditions studied

- Cholecystectomy
- Benign Hysterectomy
- Salingo-oophorectomy

## Interventions

- **DEVICE:** Cannula and Blunt Obturator

## Key facts

- **NCT ID:** NCT02163239
- **Lead sponsor:** Minimally Invasive Devices, Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** TERMINATED
- **Start date:** 2015-03
- **Primary completion:** 2015-09
- **Final completion:** 2015-09
- **Target enrollment:** 20 (ACTUAL)
- **Why stopped:** Not meeting primary objective of the study
- **Last updated:** 2015-09-28


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02163239

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02163239, "Post Market Study for FloShield 10mm Reusable Cannula and Blunt Obturator and Robotic FloShield". Retrieved via AI Analytics 2026-06-07 from https://api.ai-analytics.org/clinical/NCT02163239. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*