Trials / Terminated
TerminatedNCT02205307
A Study Assessing Perfusion Outcomes With PINPOINT® Near Infrared Fluorescence Imaging in Low Anterior Resection
A Randomized, Controlled, Parallel, Multicenter Study Assessing Perfusion Outcomes With PINPOINT® Near Infrared Fluorescence Imaging in Low Anterior Resection
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 347 (actual)
- Sponsor
- Novadaq Technologies ULC, now a part of Stryker · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a randomized, controlled, parallel, multicenter study to determine the difference in post-operative anastomotic leak rate in low anterior resection procedures where colon and rectal tissue perfusion is evaluated using PINPOINT as an adjunct to standard surgical practice compared to surgical procedures performed according to standard surgical practice alone.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | PINPOINT | |
| DEVICE | SPY Elite |
Timeline
- Start date
- 2015-01-01
- Primary completion
- 2017-05-01
- Completion
- 2017-05-01
- First posted
- 2014-07-31
- Last updated
- 2020-06-24
- Results posted
- 2020-06-24
Locations
24 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT02205307. Inclusion in this directory is not an endorsement.