UNIVERSAL DOCUMENT · TRIAL PROVENANCE

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SUPR-3D: Simple Unplanned Palliative Radiotherapy Versus 3D Conformal Radiotherapy for Patients With Bone Metastases

NCT03694015TERMINATEDChecked 2026-09-21T15:03:37.778Z
2sources
16claims traced
0observed changes
0source conflicts

OVERVIEW

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Brief TitleSUPR-3D: Simple Unplanned Palliative Radiotherapy Versus 3D Conformal Radiotherapy for Patients With Bone MetastasesPrimary source2026-09-21T15:03:37.089Z
Official TitleSUPR-3D: A Randomized Phase III Trial Comparing Simple Unplanned Palliative Radiotherapy Versus 3D Conformal Radiotherapy for Patients With Bone MetastasesPrimary source2026-09-21T15:03:37.089Z
Overall StatusTERMINATEDPrimary source2026-09-21T15:03:37.089Z
Phase["NA"]Primary source2026-09-21T15:03:37.089Z
SponsorBritish Columbia Cancer AgencyPrimary source2026-09-21T15:03:37.089Z
CollaboratorsUNKNOWNPrimary source2026-09-21T15:03:37.089Z
Enrollment160Primary source2026-09-21T15:03:37.089Z
Enrollment TypeACTUALPrimary source2026-09-21T15:03:37.089Z
Interventions[{"type":"RADIATION","name":"SUPR"},{"type":"RADIATION","name":"VMAT"}]Primary source2026-09-21T15:03:37.089Z
Conditions["Neoplasm Metastasis","Neoplastic Processes","Neoplasms","Pathologic Processes"]Primary source2026-09-21T15:03:37.089Z
Primary Outcomes[{"measure":"Patient Reported Quality of life related to Radiation Induced Nausea and Vomiting (RINV)","timeFrame":"day 1-5"}]Primary source2026-09-21T15:03:37.089Z
Secondary Outcomes[{"measure":"Control of RINV Radiation Induced Nausea and Vomiting (RINV)","timeFrame":"day 1-5"},{"measure":"Patient Reported Pain Response","timeFrame":"baseline, 2 weeks, and 4 weeks post treatment"},{"measure":"Patient Reported Use of Medications","timeFrame":"baseline, 2 weeks, and 4 weeks post treatment"},{"measure":"Patient Reported Fatigue, Nausea, Vomiting","timeFrame":"baseline, 2 weeks, and 4 weeks post treatment"},{"measure":"Patient Reported Quality of Life","timeFrame":"baseline, 2 weeks, and 4 weeks post treatment"},{"measure":"Economic Analysis","timeFrame":"baseline, 2 weeks, and 4 weeks post treatment"}]Primary source2026-09-21T15:03:37.089Z
Start Date2019-12-02Primary source2026-09-21T15:03:37.089Z
Primary Completion Date2026-02-27Primary source2026-09-21T15:03:37.089Z
Study Completion Date2026-02-27Primary source2026-09-21T15:03:37.089Z
Study TypeINTERVENTIONALPrimary source2026-09-21T15:03:37.089Z

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IntegrityINTEGRITY VERIFIED

Signer identityNOT CHECKED

TimestampLOCAL SIGNED TIME ONLY

Current statusNOT CHECKED

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