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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02314962
Other study ID # KEK ZH Nr 20140077
Secondary ID
Status Terminated
Phase N/A
First received October 23, 2014
Last updated December 15, 2016
Start date December 2014
Est. completion date December 2016

Study information

Verified date December 2016
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial Summary

Diagnostic comparison between PET/CT and PET/MRI with integrated perfusion measurement in CT and MR. Study aim is to gain knowledge about additional value of CT perfusion and MR perfusion in solid tumors concerning tumor physiology, diagnostic accuracy and possibly prognostic.


Recruitment information / eligibility

Status Terminated
Enrollment 43
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender Both
Age group 30 Years to 90 Years
Eligibility Inclusion Criteria:

- indication as stated above

- written informed consent

- patients with suspected or confirmed solid malignant tumors of the neck, chest or abdomen who have an indication for a PET/CT

Exclusion Criteria:

- pregnant or breast feeding women

- non compliance of the patient to follow the study instructions (e.g. hearing problems, dementia)

- Inclusion in another clinical trial 30 days prior to inclusion

- age < 30years

- contraindication for MRI (cardiac pacemaker, certain metal implants, claustrophobia

- known allergies to contrast CT or MRI contrast media

- patients with an glomerular filtration rate of < 60ml/min/1.73m2

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms

  • CT Perfusion and MRI Perfusion in Solid Tumors

Locations

Country Name City State
Switzerland University Hospital Zurich, Diagnostic and Interventional Radiology Zurich ZH

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Other Measurement of blood flow (mL/100 mg tissue/min) with CT-Perfusion and PET/MR-perfusion in solid tumors. 18 months No
Other Measurement of blood volume (mL/100 mg tissue) with CT-Perfusion and PET/MR-perfusion in solid tumors. 18 months No
Other Measurement of transfer constant with PET/MR-perfusion in solid tumors. 18 months No
Primary Measurement of blood flow, blood volume and transfer constant (Ktrans) with CT-Perfusion and PET/MR-perfusion in solid tumors. 18 months No
Secondary Correlation of blood flow, blood volume and transfer constant (Ktrans) measured with CT-Perfusion and PET/MR-perfusion with progression free survival in solid tumors. 18 months No