CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 106 enrolled
Drug / intervention
Cisplatin +3 moredrug
Likely dose
Cisplatin 40mg/m2from record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02031250
NCT02031250Phase 2Completed

Randomized Phase II Study of DCE-MRI-based Dose Escalation for Poor-prognosis and Neck Cancer

University of Michigan Rogel Cancer Center·interventional·Posted Jan 9, 2014·Updated Mar 2, 2026

In Brief

A Phase 2 clinical trial evaluating Cisplatin, Carboplatin, and 2 other interventions for Squamous Cell Carcinoma of the Head and Neck. Completed, enrolled 106 participants across 2 sites.

Detailed Summary

This study aims to improve locoregional control of poor prognosis Head and Neck Cancer (HNC) patients by selectively escalating the radiotherapy dose to subvolumes of tumor likely to be resistant to standard Radiation Therapy (RT) using DCE-MRI (Dynamic Contrast Enhanced Magnetic Resonance Imaging). Standard doses of radiotherapy to the rest of the tissues and surrounding normal tissues will be maintained.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJan 9, 2014
Enrollment StartFeb 1, 2014
Primary CompletionFeb 22, 2023
TodayJul 2, 2026
Enrollment to primary: 9.1 yearsPosted 12.5 years ago

Interventions

Cisplatindrug

Cisplatin 40mg/m2 administered as an IV infusion prior to radiotherapy on day 1 of each week of chemo-irradiation

Carboplatindrug

Patients considered medically unfit to receive Cisplatin as determined by the prescribing physician, will receive Carboplatin via IV infusion on day 1 of each week of chemo-irradiation

IMRT (Intensity-Modulated Radiation Therapy)radiation

Boost Radiation to Hypoperfused Volumesradiation