๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-03-25

Lanreotide Versus Placebo Before Surgery to Prevent a Surgical Complication Called a Pancreatic Fistula (NCT06807437)

A Randomized Phase III Blinded Trial of Lanreotide for the Prevention of Postoperative Pancreatic Fistula

๐ŸŸข Recruiting Phase3 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: SWOG Cancer Research Network

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This phase III trial compares the effect of using lanreotide before surgery to surgery alone in preventing pancreatic fistulas in patients with pancreatic cancer or a pancreatic lesion that could become cancerous. Lanreotide, a type of somatostatin analog similar to somatostatin (a hormone made by the body), and is used to treat certain types of gastroenteropancreatic neuroendocrine tumors, and carcinoid syndrome. It may help stop the body from making extra amounts of certain hormones, including growth hormone, insulin, glucagon, and hormones that affect digestion. It may also help keep certain types of tumor cells from growing. Patients with pancreatic cancer or pancreatic lesions may undergo surgery to remove parts of the pancreas, also called a distal pancreatectomy. Patients may experience complications after surgery, including pancreatic fistulas. A pancreatic fistula occurs when there is a small leak from the pancreas, causing fluids to collect. This can often lead to infection and other problems. Giving lanreotide before undergoing distal pancreatectomy may be more effective than surgery alone in preventing the development of a pancreatic fistula in patients with pancreatic cancer or a pancreatic lesion that could become cancerous.

Who can join: Review the eligibility criteria below.

Location: University of Alabama at Birmingham Cancer Center โ€” Birmingham, Alabama

Age range: 18 Years

๐Ÿงช Interventions in This Study

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (118 Sites)

Showing the first 25 of 118 sites.

  • University of Alabama at Birmingham Cancer Center โ€” Birmingham, Alabama
  • Gulf Health Hospitals Inc/Infirmary Cancer Care - Malbis โ€” Daphne, Alabama
  • Thomas Hospital โ€” Fairhope, Alabama
  • Mobile Infirmary Medical Center โ€” Mobile, Alabama
  • Gulf Health Hospitals Inc/Infirmary Cancer Care - Saraland โ€” Saraland, Alabama
  • Banner MD Anderson Cancer Center โ€” Gilbert, Arizona
  • City of Hope Comprehensive Cancer Center โ€” Duarte, California
  • UC San Diego Moores Cancer Center โ€” La Jolla, California
  • Veterans Affairs Loma Linda Healthcare System โ€” Loma Linda, California
  • USC / Norris Comprehensive Cancer Center โ€” Los Angeles, California
  • UC San Diego Medical Center - Hillcrest โ€” San Diego, California
  • Helen F Graham Cancer Center โ€” Newark, Delaware
  • Medical Oncology Hematology Consultants PA โ€” Newark, Delaware
  • Christiana Care Health System-Christiana Hospital โ€” Newark, Delaware
  • Christiana Care Health System-Wilmington Hospital โ€” Wilmington, Delaware
  • Moffitt Cancer Center at SouthShore โ€” Ruskin, Florida
  • Moffitt Cancer Center-International Plaza โ€” Tampa, Florida
  • Moffitt Cancer Center - McKinley Campus โ€” Tampa, Florida
  • Moffitt Cancer Center โ€” Tampa, Florida
  • Moffitt Cancer Center at Wesley Chapel โ€” Wesley Chapel, Florida
  • Grady Health System โ€” Atlanta, Georgia
  • Emory University Hospital Midtown โ€” Atlanta, Georgia
  • Emory University Hospital/Winship Cancer Institute โ€” Atlanta, Georgia
  • Emory Saint Joseph's Hospital โ€” Atlanta, Georgia
  • Emory Johns Creek Hospital โ€” Johns Creek, Georgia

๐Ÿ“ž Contact the Study Coordinator

Phone: (210) 614-8808

Email: agarcia@swog.org

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—