Actively Recruiting

Age: 18Years +
All Genders
NCT03577197

Southeast Netherlands Advanced Metastatic Breast Cancer Registry

Led by Academisch Ziekenhuis Maastricht · Updated on 2024-07-23

7000

Participants Needed

1

Research Sites

1095 weeks

Total Duration

On this page

Sponsors

A

Academisch Ziekenhuis Maastricht

Lead Sponsor

N

Novartis

Collaborating Sponsor

AI-Summary

What this Trial Is About

The Southeast Netherlands Advanced Breast Cancer (SONABRE) Registry is a real life multi-center study. The registry aims to include all patients diagnosed with advanced breast cancer as of 2007 in 11 hospitals in the Netherlands. Data on patient, tumor and treatment characteristics are collected retrospectively from electronic medical files by trained registry clerks.

CONDITIONS

Official Title

Southeast Netherlands Advanced Metastatic Breast Cancer Registry

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with de novo or recurrent advanced breast cancer since 2007
  • Diagnosed with or treated for advanced breast cancer in one of the participating hospitals
  • Participating hospitals and inclusion periods: Maastricht UMC+ (2007-2025), Zuyderland hospitals Sittard/Heerlen (2007-2025), Amphia Hospital Breda (2013-2025), Catharina Hospital Eindhoven (2007-2025), Elkerliek Hospital Helmond (2010-2025), Maxima Medical Center Veldhoven/Eindhoven (2007-2025), Jeroen Bosch Hospital Den Bosch (2013-2025), Laurentius Hospital Roermond (2007-2025), St. Annaziekenhuis Geldrop (2007-2025), St. Elisabeth Hospital Tilburg (2007-2009), St. Jans Gasthuis Weert (2007-2025), VieCuri Medical Center Venlo/Venray (2013-2025), all in the Netherlands
  • Hospitals (and periods) were eligible for inclusion if distant registration from Maastricht UMC+ was possible
  • The inclusion period may be prolonged after 2025
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 1 location

1

Multiple hospitals in the Netherlands (see Eligibility)

Maastricht, Netherlands

Actively Recruiting

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Research Team

V

Vivianne CG Tjan-Heijnen, MD, PhD

CONTACT

S

Sandra ME Geurts, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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