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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03367065
Other study ID # PERFE-CT
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2016
Est. completion date December 2017

Study information

Verified date April 2020
Source Poitiers University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This feasibility study has therefore several aims:

1. construct a dedicated CT perfusion protocol for GIT wall perfusion;

2. used a two-compartment pharmacokinetic model which is more adapted that a unique compartment model;

3. from the image acquired, evaluate current parameters of perfusion including the permeability ones


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date December 2017
Est. primary completion date November 2017
Accepts healthy volunteers No
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria:

- all patients over fifty years old with clinico-biological suspicion for acute GITischemia admitted at our institution

Exclusion Criteria:

- contra-indication to contrast agent injection as so defined by the European Society of UroRadiology in 2014

- inability to provide informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
Dynamic contrast enhanced computerised tomography


Locations

Country Name City State
France Chu Poitiers Poitiers Aquitaine

Sponsors (1)

Lead Sponsor Collaborator
Poitiers University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of computerised tomography with interpretable data 2 hours
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