Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

The DRAGON 2 Trial

NCT05428735 · View on ClinicalTrials.gov ↗

Study Summary

In the randomized controlled DRAGON 2 trial study subjects will be randomized between two arms, PVE alone (control group) and PVE/HVE (interventional group).

Interventions

  • PROCEDURE Embolization

Study Locations (20)

Other

  • McGill University Health Center — Montreal
  • IRCCS San Raffaele Hospital — Milan
  • Amphia — Breda
  • Maxima Medisch Centrum — Eindhoven
  • Universitair Medisch Centrum Utrecht — Utrecht

Ontario

  • Juravinski Hospital and Cancer Centre — Hamilton
  • The Ottawa Hospital — Ottawa
  • Sunnybrook Hospital — Toronto

Connecticut

  • Yale New Haven Hospital — New Haven

Victoria

  • Monash Medical Centre — Clayton

Vienna

  • Social Medical Center, South — Vienna

Brussels Capital

  • Hôpital Erasme — Brussels

Liège

  • CHU de Liège — Liège

Namen

  • CHU-UCL Namur site Godinne — Yvoir

Trial Details

FieldValue
Enrollment Target 348 participants
Start Date 2022-04-01
Est. Completion 2029-06-30
Phase NA

Sponsor

Maastricht University

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05428735

The ClinicalTrials.gov registry entry for NCT05428735 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 348 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Maastricht University, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Colorectal Cancer Liver Metastases (CRLM) appearing as the primary indexed condition, and to 1 intervention — of which Embolization is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05428735 reports 20 study locations spanning 14 distinct geographic areas — top geographies include Other, Ontario, Connecticut. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05428735 about?

NCT05428735 is a clinical study titled "The DRAGON 2 Trial". In the randomized controlled DRAGON 2 trial study subjects will be randomized between two arms, PVE alone (control group) and PVE/HVE (interventional group).

What is the current status of trial NCT05428735?

This trial is currently recruiting. It is a NA study. The enrollment target is 348 participants. The study started on 2022-04-01. Estimated completion is 2029-06-30.

What conditions does trial NCT05428735 study?

This clinical trial studies the following conditions: Colorectal Cancer Liver Metastases (CRLM), Small Future Liver Remnant (FLR). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05428735?

The interventions under investigation include: Embolization (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05428735?

This trial is sponsored by Maastricht University, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05428735 being conducted?

This trial has 20 study locations across Connecticut, Victoria, Vienna, Brussels Capital, Liège. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial