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NCT02790983Recruiting

Primary Tumor Research and Outcomes Network

Primary Tumor Research and Outcomes Network (PTRON) A Multicenter Prospective Registry for the Management and Outcomes of Primary Tumors of the Spine

Source: ClinicalTrials.gov · Last updated 25 Feb 2026

Brief summary (registry, in English)

This project aims to establish a network of spine oncology centers dedicated to prospective multicenter research of patients diagnosed with a primary tumor of the spine and will include a comprehensive prospective clinical database which will serve as a shared research platform. Demographic, clinical, diagnostic, and therapeutic variables will be used to answer questions about survival and local recurrence, as well as questions about adverse events (AEs), morbidity data, and health-related quality of life (HRQOL) outcomes.

Status (registry)
Recruiting
Study type
Observational
Enrollment
1350 (estimated)
First submitted
18 May 2016
Start date
Oct 2016
Primary completion date
Dec 2028
Lead sponsor
AO Innovation Translation Center
NCT number
NCT02790983

What you commit to

  • Study type: Observational
  • Planned participants: 1350
  • From Oct 2016 to the primary completion date, Dec 2028
  • 18 sites in 9 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • \- Patient diagnosed with a metastatic tumor of the spine.

Who the study is looking for

  • Patient with a current primary spine tumor or history of a primary spine tumor, including tumors within or surrounding the spinal column and/or spinal cord. This includes extradural tumors, intramedullary tumors (i.e. astrocytomas, ependymoma, etc.) and extramedullary tumors (i.e. meningiomas, neurofibromas, schwannomas, etc.).
  • Informed consent obtained, i.e.:
    • Ability to understand the content of the patient information/ICF
    • Willingness and ability to participate in the registry according to the Registry Plan (RP)
    • Signed and dated EC/IRB approved written informed consent
    • OR
  • Written consent provided according to the IRB/EC defined and approved procedures for patients who are not able to provide independent written informed consent

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (18)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Queensland, School of Medicine
Coordinator of this site? Confirm its status
BrisbaneAustraliaWithdrawn
Toronto Western Hospital
Coordinator of this site? Confirm its status
TorontoCanadaTerminated
Vancouver General Hospital and the University of British Columbia
Coordinator of this site? Confirm its status
VancouverCanadaRecruiting
Peking University 3rd Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting
Universitaetsklinikum Carl Gustav Carus der Techn. Universitaet - Dresden
Coordinator of this site? Confirm its status
DresdenGermanyRecruiting
Oxford University Hospitals
Coordinator of this site? Confirm its status
OxfordUnited KingdomRecruiting
National Center for Spinal Disorders and Buda Health Center
Coordinator of this site? Confirm its status
BudapestHungaryRecruiting
Istituto Ortopedico Rizzoli
Coordinator of this site? Confirm its status
BolognaItalyRecruiting
IRCCS Istituto Ortopedico Galeazzi
Coordinator of this site? Confirm its status
MilanItalyRecruiting
Kanazawa Medical University Hospital
Coordinator of this site? Confirm its status
KanazawaJapanTerminated
Johns Hopkins University School Of Medicine
Coordinator of this site? Confirm its status
BaltimoreUnited StatesRecruiting
Massachusetts General Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesRecruiting
The University of Texas M. D. Anderson Cancer Center
Coordinator of this site? Confirm its status
HoustonUnited StatesRecruiting
University of California
Coordinator of this site? Confirm its status
Los AngelesUnited StatesTerminated
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesWithdrawn
Rhode Island Hospital
Coordinator of this site? Confirm its status
ProvidenceUnited StatesRecruiting
Mayo Clinic
Coordinator of this site? Confirm its status
RochesterUnited StatesRecruiting
UCSF Medical Center
Coordinator of this site? Confirm its status
San FranciscoUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.