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Terminated Not applicable Interventional Results available

A Study Assessing Perfusion Outcomes With PINPOINT® Near Infrared Fluorescence Imaging in Low Anterior Resection

ClinicalTrials.gov ID: NCT02205307

Public ClinicalTrials.gov record NCT02205307. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 10:00 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Controlled, Parallel, Multicenter Study Assessing Perfusion Outcomes With PINPOINT® Near Infrared Fluorescence Imaging in Low Anterior Resection

Study identification

NCT ID
NCT02205307
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
Novadaq Technologies ULC, now a part of Stryker
Industry
Enrollment
347 participants

Conditions and interventions

Interventions

  • PINPOINT Device
  • SPY Elite Device

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 31, 2014
Primary completion
Apr 30, 2017
Completion
Apr 30, 2017
Last update posted
Jun 23, 2020

2015 – 2017

United States locations

U.S. sites
24
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
John Muir Medical Center, Concord Campus Concord California
Kaiser Permanente Los Angeles California
University of California, Irvine Orange California
University of California, San Francisco San Francisco California
Mayo Clinic - Jacksonville Jacksonville Florida
University of South Florida Tampa Florida
Cleveland Clinic Florida Weston Florida
Rush University Medical Center Chicago Illinois
Indiana University Indianapolis Indiana
Ochsner Clinic New Orleans Louisiana 70121
Johns Hopkins Baltimore Maryland
Massachusetts General Hospital Boston Massachusetts
Barnes Jewish Medical Center St Louis Missouri
Sunrise Hospital and Medical Center Las Vegas Nevada 89109
Mount Sinai Beth Israel New York New York 10003
Mount Sinai Medical Center New York New York
Weill Cornell Medical College New York New York
The Christ Hospital Cincinnati Ohio
Cleveland Clinic Cleveland Ohio
University Hospitals Cleveland Medical Center Cleveland Ohio
Medical University of South Carolina Charleston South Carolina
Vanderbilt University Medical Center Nashville Tennessee
Baylor University Medical Center Dallas Texas 75246
Methodist Hospital Houston Texas

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02205307, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 23, 2020 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02205307 live on ClinicalTrials.gov.

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