The MOMENTUM Study: The Multiple Outcome Evaluation of Radiation Therapy Using the MR-Linac Study

NCT04075305 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 8000

Last updated 2026-03-05

No results posted yet for this study

Summary

The Multi-OutcoMe EvaluatioN of radiation Therapy Using the Unity MR-Linac Study (MOMENTUM) is a multi-institutional, international registry facilitating evidenced based implementation of the Unity MR-Linac technology and further technical development of the MR-Linac system with the ultimate purpose to improve patients' survival, local, and regional tumor control and quality of life.

Conditions

Interventions

RADIATION

Radiation therapy

Radiation therapy on the CE marked and FDA approved MR-Linac

Sponsors & Collaborators

  • The Netherlands Cancer Institute

    collaborator OTHER
  • Sunnybrook Health Sciences Centre

    collaborator OTHER
  • M.D. Anderson Cancer Center

    collaborator OTHER
  • The Christie NHS Foundation Trust

    collaborator OTHER
  • Royal Marsden NHS Foundation Trust

    collaborator OTHER
  • Medical College of Wisconsin

    collaborator OTHER
  • Elekta Limited

    collaborator INDUSTRY
  • Odense University Hospital

    collaborator OTHER
  • Radboud University Medical Center

    collaborator OTHER
  • Radiotherapiegroep

    collaborator OTHER
  • Jules Bordet Institute

    collaborator OTHER
  • University Hospital Tuebingen

    collaborator OTHER
  • Radiotherapeutic Institute Friesland

    collaborator OTHER
  • Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)

    collaborator OTHER
  • IRCCS Sacro Cuore Don Calabria di Negrar

    collaborator OTHER
  • Austin Health

    collaborator OTHER_GOV
  • Princess Margaret Hospital, Canada

    collaborator OTHER
  • Università degli Studi di Brescia

    collaborator OTHER
  • UMC Utrecht

    lead OTHER

Principal Investigators

  • Helena M Verkooijen, Prof, Dr · Universitair Medical Centre Utrecht

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-01
Primary Completion
2030-02-01
Completion
2030-08-01
FDA Device
Yes

Countries

  • United States
  • Australia
  • Belgium
  • Canada
  • Denmark
  • Germany
  • Italy
  • Netherlands
  • United Kingdom

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04075305 on ClinicalTrials.gov