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NCT06586892: (QI-ProVE-MRI)

Quantitative Imaging Biomarker Prospective Validation of Dynamic Contrast-enhanced MRI as a Metric of Orodental Injury After Radiotherapy (QI-ProVE-MRI)

Recruiting now Last updated 4 March 2026
What this trial tests

trial testing Radiotherapy followed by chemotherapy in Orodental Injury in 300 participants. Currently enrolling.

Timeline
15 September 2025
Primary endpoint
30 December 2030
30 December 2032

Quick facts

Lead sponsorM.D. Anderson Cancer Center
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment300
Start date15 September 2025
Primary completion30 December 2030
Estimated completion30 December 2032
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

M.D. Anderson Cancer Center — full company profile →

Who can join

18 and older, any sex, with Orodental Injury. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This research will focus on the prospective qualification and validation of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) candidate biomarkers (i.e., Ktrans and Ve) to assess the natural history of osteoradionecrosis (ORN) and treatment for this devastating complication related to irradiation of head and neck cancers. The investigations will also include assessment of DCE-MRI candidate biomarkers for pre-qualification as quantitative imaging biomarkers of soft-tissue structures.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Radiotherapy followed by chemotherapy

Trials testing the same drug.

Other M.D. Anderson Cancer Center trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06586892.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing