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Study identifier: NCT07656571 Synced from ClinicalTrials.gov · July 28, 2026
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Indocyanine Green-Guided Versus Standard Laparoscopic Distal Pancreatectomy for Pancreatic Body and Tail Lesions

Condition: Pancreatic Neoplasms · Pancreatic Cancer  ·  Sponsor: Alexandria University

PhaseNA
Planned participants72
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Postoperative pancreatic fistula is the most important complication after laparoscopic distal pancreatectomy for tumors of the body and tail of the pancreas. It can cause infection, bleeding, longer hospital stay, and even death. New imaging technology using indocyanine green (ICG) dye and near-infrared fluorescence may help surgeons see blood flow to the pancreatic stump, spleen, and nearby vessels during surgery and make safer decisions about where to cut and which structures to preserve. This study will compare two standard laparoscopic operations for pancreatic body and tail lesions: one with ICG fluorescence imaging at key steps of the procedure and one without ICG imaging. Adult patients who need elective laparoscopic distal pancreatectomy will be randomly assigned to one of the two groups. All other aspects of care before, during, and after surgery will be the same. The main goal is to find out whether using ICG fluorescence can reduce the rate of clinically relevant postoperative pancreatic fistula (Grade B or C) within 90 days after surgery. Secondary goals include comparing blood loss, operating time, need to convert to open surgery, spleen preservation, complications, hospital stay, and oncologic outcomes such as margin status and lymph node yield.

This description comes directly from the study's public registry record.

Talk to the study team

Ahmed M Farid, Lecturer, MD, MS  ·  +20227196753  ·  ahmed.farid@alexmed.edu.eg

Mohamed I Kassem, Professor, MD  ·  +201001224750

Always discuss trial participation with your own doctor first.

Locations (1)

Faculty of Medicine, Alexandria UniversityAlexandria, EgyptRecruiting

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Source record: clinicaltrials.gov/study/NCT07656571