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Clinical Trials/NCT02547610
NCT02547610
Unknown
Not Applicable

MR/PET in the Evaluation of Patients With Esophageal Cancer

National Taiwan University Hospital1 site in 1 country80 target enrollmentMay 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Esophageal Cancer
Sponsor
National Taiwan University Hospital
Enrollment
80
Locations
1
Primary Endpoint
The imaging biomarkers determined by MR-PET
Last Updated
8 years ago

Overview

Brief Summary

In this prospective study, we will recruit newly diagnosed esophageal cancer patients and perform MR/PET before and after chemoradiation therapy. In MR, new image sequences will be added to the conventional sequences, such as high resolution image, DWI, DCE, cine imaging.

Detailed Description

Total 80 patients will be recruited and followed after treatment complete for at least two years. We will compare the staging accuracy of MR/PET and PET/CT, and also analyze parameters that are predictive of disease recurrence and patient survival.

Registry
clinicaltrials.gov
Start Date
May 2014
End Date
April 2018
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • newly diagnosed esophageal cancer patient
  • age older than 20 years

Exclusion Criteria

  • For the safety reason, patients with the following conditions are contraindicated to enter magnetic resonance imaging (MRI) machine due to the high magnetic field, including: cardiac pacemaker, metallic artificial valve, intracranial and mediastinal vascular clips, cardiac defibrillator, nerve stimulator, implanted drug deliver system, metallic foreign body in the eye globe, cochlear implant, metallic fragments in the dangerous body part, Swan-Ganz catheter, and other metallic implants within 8 weeks: such as cardiac valve, stent, coil, filter, and clips.
  • patient who will receive endoscopic local therapy alone
  • unable to finish the standard surgical or radiation treatment
  • history of surgery or radiotherapy to the mediastinum
  • renal insufficiency, contraindication to MR imaging and contrast injection patient who have the severe allergic reaction the Gadollium contrast agent
  • patient who have the claustrophobic symptoms are also not suitable for this MR examination
  • pregnancy or lactating women

Outcomes

Primary Outcomes

The imaging biomarkers determined by MR-PET

Time Frame: 1 month

Study Sites (1)

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