Perfusion Assessment in Laparoscopic Left Anterior Resection

ClinicalTrials.gov ID: NCT01560377

Public ClinicalTrials.gov record NCT01560377. 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.

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ClinicalTrials.gov public records Last synced Jul 21, 2026, 4:49 PM EDT

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

Official title

Open Label Clinical Study to Demonstrate the Utility of Intra-operative Perfusion Assessment Using NIR Fluorescence Angiography With the PINPOINT® Endoscopic Fluorescence Imaging System and to Assess the Impact of PINPOINT on the Surgical Decision Making Process and on Surgical Outcomes in Laparoscopic Left Anterior Resection Procedures

Study identification

NCT ID: NCT01560377
Recruitment status: Completed
Study type: Interventional
Phase: Phase 1
Lead sponsor: Novadaq Technologies ULC, now a part of Stryker; Industry
Enrollment: 147 participants

Conditions and interventions

Conditions

Interventions

PINPOINT Endoscopic Fluorescence Imaging System 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: Apr 30, 2012
Primary completion: Sep 30, 2013
Completion: Oct 31, 2013
Last update posted: Dec 10, 2018

2012 – 2013

United States locations

U.S. sites: 11
U.S. states: 6
U.S. cities: 10

Facility	City	State	ZIP	Site status
University of Southern California	Los Angeles	California	90089	—
University of California, Irvine	Orange	California	92868	—
University of California San Diego	San Diego	California	92093	—
University of California San Francisco	San Francisco	California	94115	—
Cleveland Clinic Florida	Weston	Florida	33331	—
Ochsner Medical Center	New Orleans	Louisiana	70121	—
Mayo Clinic	Rochester	Minnesota	55905	—
Maimonides Medical Center	Brooklyn	New York	11219	—
Beth Israel Medical Center	New York	New York	10003	—
Weill Cornell Medical College	New York	New York	10021	—
University Hospital Case Medical Center	Cleveland	Ohio	44106	—

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 NCT01560377, 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 Dec 10, 2018 · Synced Jul 21, 2026

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01560377 live on ClinicalTrials.gov.

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