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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01276483
Other study ID # REK-2010/2089
Secondary ID
Status Completed
Phase N/A
First received January 12, 2011
Last updated June 21, 2017
Start date February 2011
Est. completion date June 21, 2017

Study information

Verified date June 2017
Source Oslo University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to compare sensitivity, specificity and accuracy of PET, DW MRI and CT separately and combined for the evaluation of treatment response and progression-free survival in patients with GIST.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date June 21, 2017
Est. primary completion date June 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Metastatic GIST patients suitable for TKI treatment

- GIST patients pursuing preoperative neoadjuvant TKI treatment

Exclusion Criteria:

- Patients with contraindications to MRI and/or TKI treatment. For patients with renal failure, CT without intravenous contrast will be performed according to clinical practice.

- Patients who do not sign the consent paper for any reason or do not accept the study premises or patients who wish to withdraw for any reason during the study

Study Design


Locations

Country Name City State
Norway Oslo University Hosptal Oslo

Sponsors (1)

Lead Sponsor Collaborator
Oslo University Hospital

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Radiologic-pathologic correlation 2 years
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