BSMO Oncology

Welcome

The aim of this website is to provide Belgian oncologists with swift access to clinical trial opportunities for their patients, with the possibility to directly contact one of the sites where the trial is open.

This search portal combines a structured national database with intuitive filters by disease, centre, molecule and report extraction to help clinicians identify relevant trials efficiently.

The methodology relies on curated Belgian trial data and a practical search interface designed to make navigation clear, fast and clinically useful.

Main scientific and medical input: Dr. Cédric van Marcke, Dr Joëlle Collignon and Dr Hans Prenen, as well as several other oncologists.

What are Clinical Trials?

Clinical trials are a key step in the development and evaluation of new treatments.

Before a new treatment reaches routine care, it is studied through carefully designed research. Patients who participate receive information about the study, its possible benefits, its risks and the alternatives before giving informed consent.

Phases in clinical trials

Phase I

Early studies focus mainly on safety, dosage and initial signs of activity.

Phase II

A larger group is studied to better assess efficacy and adverse events.

Phase III

The new approach is compared with existing standards in a larger patient population.

Phase IV

Post-marketing studies can evaluate longer-term outcomes and rarer adverse events.

Should I participate in a clinical trial?

Participation is a personal medical decision that should be discussed with the treating team. A trial may offer access to a promising treatment and close follow-up, but it may also involve uncertainty, extra visits, tests or unexpected side effects.

Potential benefits

  • Early access to a promising treatment.
  • Structured follow-up within a research programme.
  • Contribution to better future cancer care.

Potential risks

  • The new treatment may not work better than standard care.
  • Unexpected adverse events can occur.
  • Participation can require extra procedures or visits.

Informed consent

Before joining a study, patients receive information about the trial, potential benefits, risks and alternatives. Participation remains voluntary and consent can be withdrawn.

How to submit or update a trial?

Professionals may request the addition or update of a trial running in Belgium. Recruitment status, site details, investigator information and approved supporting material should be kept current.

Only material that has the required ethics and sponsor approval should be published.

For trial updates or missing studies, contact info@clinicaltrial.be.