ClinicalTrials.Veeva

Menu

MR/PET in the Evaluation of Patients With Esophageal Cancer

National Taiwan University logo

National Taiwan University

Status

Unknown

Conditions

Esophageal Cancer

Treatments

Device: The imaging biomarkers determined by MR-PET

Study type

Observational

Funder types

Other

Identifiers

NCT02547610
201402050MINC

Details and patient eligibility

About

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.

Full 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.

Enrollment

80 estimated patients

Sex

All

Ages

20 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. newly diagnosed esophageal cancer patient
  2. age older than 20 years

Exclusion criteria

  1. 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.
  2. patient who will receive endoscopic local therapy alone
  3. unable to finish the standard surgical or radiation treatment
  4. history of surgery or radiotherapy to the mediastinum
  5. renal insufficiency, contraindication to MR imaging and contrast injection patient who have the severe allergic reaction the Gadollium contrast agent
  6. patient who have the claustrophobic symptoms are also not suitable for this MR examination
  7. pregnancy or lactating women

Trial contacts and locations

1

Loading...

Central trial contact

Ting-Fang Shih, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems