The DRAGON 2 Trial (NCT05428735)
An International Multicenter Randomized Controlled Trial to Compare Combined Portal and Hepatic Vein Embolization (PVE/HVE) with PVE Alone in Patients with Colorectal Liver Cancer Metastases (CRLM) and a Small Future Liver Remnant (FLR)
🩺 Plain-English Summary (8th-Grade Level)
In the randomized controlled DRAGON 2 trial study subjects will be randomized between two arms, PVE alone (control group) and PVE/HVE (interventional group).
Who can join: Review the eligibility criteria below.
Location: Yale New Haven Hospital — New Haven, Connecticut
Age range: 18 Years
🧪 Interventions in This Study
- Embolization (PROCEDURE)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (24 Sites)
- Yale New Haven Hospital — New Haven, Connecticut
- Monash Medical Centre — Clayton, Victoria
- Social Medical Center, South — Vienna, State of Vienna
- Hôpital Erasme — Brussels, Brussels Capital
- CHU de Liège — Liège, Liège
- CHU-UCL Namur site Godinne — Yvoir, Namen
- UZ Gent — Ghent, Oost-Vlaanderen
- Vancouver Coastal Health — Vancouver, British Columbia
- Juravinski Hospital and Cancer Centre — Hamilton, Ontario
- The Ottawa Hospital — Ottawa, Ontario
- Sunnybrook Hospital — Toronto, Ontario
- McGill University Health Center — Montreal,
- IRCCS San Raffaele Hospital — Milan,
- Maastricht University Medical Center+ — Maastricht, Limburg
- Amsterdam UMC, location AMC — Amsterdam, North Holland
- University Medical Center Groningen — Groningen, Provincie Groningen
- Erasmus Medical Center — Rotterdam, South Holland
- Amphia — Breda,
- Maxima Medisch Centrum — Eindhoven,
- Universitair Medisch Centrum Utrecht — Utrecht,
- Linköping University Hospital — Linköping,
- Karolinska University Hospital — Stockholm,
- Claraspital & Clarunis University Hospital Basel — Basel, Canton of Basel-City
- Kantonsspital Winterthur (KSW) — Winterthur,
📞 Contact the Study Coordinator
Phone: +31 638463945
Email: sinead.james@mumc.nl
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 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 § 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.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.