Minimally Invasive Imagery With Indocyanine Green

Completed · Phase 1

Conditions studied: Neoplasms

In brief

Determine if ICG administered pre-operatively, then imaged intraoperatively using our cameras, will aid in the identification of a suspected thoracic nodules, margins, lymph nodes and satellite nodules during minimally invasive procedures. The investigators intend on enrolling 48 Subjects in this study. The study is focusing on patients presenting with suspected thoracic cancers who are considered to be good minimally invasive surgical candidates

Key facts

Study ID

NCT02621268

Run by

University of Pennsylvania

People needed

48

Starts

2014-11-01

Expected to finish

2016-11-01

Last updated by the study team

2018-03-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adult patients over 18 years of age
• Patients presenting with a thoracic nodule presumed to be resectable cancer on pre-operative assessment
• Good minimally invasive operative candidates as determined by a thoracic oncology multidisciplinary team
• Subject capable of giving informed consent and participating in the process of consent.

You may not qualify if…

• Pregnant women as determined by urinary or serum beta human chorionic gonadotropin (hCG) within 72 hours of surgery
• Subjects with a history of iodide allergies
• At-risk patient populations
• Homeless patients
• Patients with drug or alcohol dependence
• Children and neonates
• Patients unable to participate in the consent process

Where it is running

• Hospital of the University of Pennsylvania — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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