Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
1000 participants
OBSERVATIONAL
2019-07-29
2029-04-02
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Short Course Of Preoperative Radiotherapy in Head and Neck-, Trunk- and Extremity Soft Tissue Sarcomas
NCT04425967
Advanced MR Imaging in Sarcoma Patients
NCT02705391
Stereotactic Radiosurgery for Soft Tissue Sarcoma
NCT02706171
Lymphatic Mapping for Image Guided Radiotherapy in Patients With LACC - a Feasibility Study
NCT05746156
High Versus Lower Intensity Surveillance Following Resection of Retroperitoneal Sarcoma
NCT06480396
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
* To improve the knowledge and therefore the treatment care, in patients with bone or soft tissue sarcoma in the Netherlands
* To start an observational cohort study of bone and soft tissue sarcoma patients from their primary diagnosis until death
* To prospectively and retrospectively collect data on medical history, co-morbidities, baseline clinical parameters, imaging results, pathology results, tumor characteristics, treatment, treatment outcomes, functional outcome, cosmetic outcome, hospital stays and interventions.
* To collect data on health related quality of life and work ability, to collect data on patient reported outcomes measures.
* To create a continuous basis for a large variety of research purposes including:
* Prognostic and predictive research
* Health care policies and cost-effectiveness studies
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
CROSS_SECTIONAL
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Surgery
all interventions are allowed
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Radiotherapiegroep
OTHER
Radboud University Medical Center
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Radiotherapiegroep
Arnhem, , Netherlands
Radboudumc
Nijmegen, , Netherlands
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Marjan van Hezewijk, MD/PhD
Role: primary
Pètra Braam, MD/PhD
Role: primary
Ingrid Desar, MD/PhD
Role: backup
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
NL69559.091.19
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.