Perfusion Assessment in Laparoscopic Left Anterior Resection



Status:Completed
Conditions:Colorectal Cancer, Colorectal Cancer, Cancer, Cancer, Gastrointestinal, Gastrointestinal, Crohns Disease, Diverticulitis
Therapuetic Areas:Gastroenterology, Oncology
Healthy:No
Age Range:18 - Any
Updated:12/13/2018
Start Date:May 2012
End Date:November 2013

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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

The purpose of this study is to demonstrate that NIR fluorescence angiography using the
PINPOINT Endoscopic Fluorescence Imaging System ("PINPOINT System" or "PINPOINT") can assess
viability of colon tissue during laparoscopic left colectomy. This information will provide
the surgeon with clinically relevant information in assessing whether or not the tissue has
adequate blood supply in the lower section of the colon prior to a colectomy.

Colectomy is a surgical procedure in which a part or all of the colon is removed. It is used
to treat a variety of diseases including colon cancer, diverticulitis, inflammatory bowel
disease (including ulcerative colitis or Crohn's disease) and infarcted bowel.

This study is the second phase of a three phase process to demonstrate the clinical utility
of perfusion assessment by NIR fluorescence angiography in colectomy. The initial phase
(Phase I) consisted of a number of small investigative studies that have now been completed.
Upon successful completion of this study, it is anticipated that a prospective, multi center,
randomized trial will be conducted (Phase III). Information learned from this present study
will help guide the design of the randomized trial e.g. specific patient populations that may
best benefit from this imaging modality and how randomization should be conducted (e.g.
imaged cohort vs. non imaged, or all subjects imaged but then randomized to no image
assessment in one arm of the study).

Inclusion Criteria:

- Subject is scheduled for laparoscopic left colectomy in the lower region (planned
anastomosis located 5 - 15 cm from anal verge)

- A negative pregnancy test for women of childbearing potential prior to surgery

Exclusion Criteria:

- Subject has a previous history of adverse reaction or known allergy to ICG, iodine or
iodine dyes

- Subject has any medical condition, which in the judgment of the Investigator and/or
designee makes the subject a poor candidate for the investigational procedure

- Subject is a pregnant or lactating female
We found this trial at
11
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Los Angeles, California 90033
213) 740-2311
University of Southern California The University of Southern California is one of the world’s leading...
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Los Angeles, CA
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305 1st Avenue # Dazian 7
New York, New York 10003
(212) 420-2806
Beth Israel Med Ctr The physicians and staff of Mount Sinai Beth Israel's Heart Institute...
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New York, NY
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2950 Cleveland Clinic Blvd.
Weston, Florida 33331
866.293.7866
Cleveland Clinic Florida Cleveland Clinic Florida, located in Weston, West Palm Beach, Palm Beach Gardens...
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Weston, FL
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4802 10th Ave
Brooklyn, New York 11219
(718) 283-6000
Maimonides Medical Center At 103 years old, Maimonides Medical Center remains a vital and thriving...
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Brooklyn, NY
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1514 Jefferson Hwy.
New Orleans, Louisiana 70121
504-842-3000
Ochsner Medical Center Ochsner Medical Center is located near uptown New Orleans and includes acute...
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New Orleans, LA
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New York, New York 10021
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New York, NY
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Orange, California 92868
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Orange, CA
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Rochester, Minnesota 55905
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Rochester, MN
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San Diego, California 92093
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San Diego, CA
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San Francisco, California 94143
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San Francisco, CA
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