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CompletedNot applicableNCT02340715
Official study title

Advanced MRI Sequences for Radiation Therapy Treatment Planning

Study summary

The purpose of this study is to determine if it would be helpful to use advanced MRI imaging techniques to take additional views of the tumor target for radiation treatment planning or treatment follow-up MRI.

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Key things to know

Main goalNot specified

This describes the study’s primary purpose.

What is being studiedNot specified

The study team can explain what participation involves.

Who it may be forCancer

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Oct 31, 2017 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Observational

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?Medical College of Wisconsin

Study sponsor

01
Study overview

What this study is about

Purpose
Not specified
Study type
Observational
Phase
Not applicable
Sponsor
Medical College of Wisconsin
Interventions being studied
Not specified
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

Treatment approach
Radiation therapy→
03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria
  • Patients aged 18 years older of any race or gender with anal canal, brain, breast, cervix, esophagus, gynecology, head and neck, lung, pancreas, primary liver or liver metastases, prostate cancer or sarcoma either undergoing MRI scan for radiation treatment planning or a post treatment MRI
  • Voluntarily signs an IRB approved consent form
Reasons someone may not be able to joinExclusion criteria
  • Inability to obtain informed consent from the patient or their medical power of attorney
  • Patients who are not undergoing MR for radiation treatment planning
  • Patients who will not have MRI scans after treatment
  • Patients with pacemakers or other non-MRI compatible metallic implants
  • Pregnant women, by self report using a standard MRI questionnaire
  • Patients who will not receive contrast agent as part of their standard MR, will participate only in the non-contrast portion of the study

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Froedtert HospitalMilwaukee, Wisconsin

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Oct 31, 2017. Always confirm current availability with the study team.

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