Use Of Indocyanine Green In Pancreas Surgery
Recruiting now
Conditions studied: Pancreatic Carcinoma
In brief
This study evaluates the use of indocyanine green to predict postoperative pancreatic leaks in patients undergoing transection of the pancreas.
Key facts
- Study ID
- NCT06084013
- Run by
- OHSU Knight Cancer Institute
- People needed
- 55
- Starts
- 2024-05-17
- Expected to finish
- 2028-02-28
- Last updated by the study team
- 2026-07-09
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Participant scheduled for open pancreaticoduodenectomy or distal pancreatectomy for any diagnosis
- Participant ≥ 18 years of age
- Ability to understand nature and individual consequences of clinical trial
- Written informed consent from participant or legally authorized representative
- For participants of childbearing potential, a negative pregnancy test and adequate contraception until 14 days after trial intervention
- Participant needs to have an operative drain (any closed suction drain) after the procedure
- Participants that do not require arterial reconstruction
- Participants that require minor portal venous recounstructions including patch venoplasty
You may not qualify if…
- Patients with previous history of adverse reaction to contrast dye, ICG or components of the dye
- Prior pancreatectomy
- Known diagnosis of hepatic insufficiency, hepatitis, liver fibrosis or cirrhosis, or chronic pancreatitis
- Because this study focuses on hypoperfusion, patients will be excluded if in postoperative day 3-5 had any of the following: persistent SBP <90 mmHg unresponsive to 1L crystalloid, unexpected ICU transfer, blood transfusion of >2 units intraoperatively or 1 postoperatively, vasopressor treatment or ACLS protocol initiation
- Organ failure, anuria or NSQIP-identified complication will be reviewed by PI and attending surgeon and excluded
- Patients that require arterial reconstruction as part of their procedures
Where it is running
- OHSU Knight Cancer Institute — Portland, Oregon, United States (enrolling)
Full record on ClinicalTrials.gov
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