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Clinical Application of MR-PET in Non-small Cell Lung Cancer: Diagnosis, Treatment Outcome, and Prognosis Prediction

Clinical Application of MR-PET in Non-small Cell Lung Cancer: Diagnosis, Treatment, Outcome, and Prognosis Prediction

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03053804
Enrollment
75
Registered
2017-02-15
Start date
2015-03-31
Completion date
2018-12-31
Last updated
2017-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-small Cell Lung Cancer

Keywords

MR/PET, Non-small cell lung cancer (NSCLC)

Brief summary

It is a study that hypothesize that MR/PET can have better information than current CT image study, about the medical or surgical treatment outcome of lung cancer

Detailed description

The investigators analyze tumor size、ADCmean、ADCmin、DCE、SUVmax、SUVmin、etc in MR/PET study,to compare its efficacy with other image studies in tumor malignancy grade, systemic involvement detection, treatment outcome after medical target therapy and treatment outcome after surgery.

Interventions

RADIATIONMR/PET

MR/PET with contrast media and FDG-18

Sponsors

National Taiwan University Hospital, Yun-Lin Branch
CollaboratorOTHER
National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

1. Age: \> 20 years old. 2. Patients have confirmed lung cancer by histopathological methods (fiber, bronchoscopy, lung biopsy, open chest biopsy, pleural effusion exfoliated cells, sputum exfoliated cells) 3. Patients voluntarily to join this study and signed informed consents.

Exclusion criteria

1. Any body metal implants (pacemaker implantation, nerve stimulator, vascular stent, aneurysm clip, eye foreign body, the inner metal prosthesis) or artificial heart valves 2. Patients with claustrophobia to MRI examination 3. Patients who are reluctant to comply with follow-up and subsequent examination 4. The other condition that do not meet the inclusion criteria. 5. Pregnancy. 6. Age \< 20 years old.

Design outcomes

Primary

MeasureTime frame
Change from Baseline PET/MR parameters at 2 months after treatment2 months after treatment

Countries

Taiwan

Contacts

Primary ContactYeun-Chung Chang
ycc5566@ntu.edu.tw02-23123456*65566
Backup ContactYu-Sen Huang
yusen0814@gmail.com02-23123456*65566

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026