Imaging of Dissection of the Descending Aorta

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

89 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-05-31

Study Completion Date

2019-08-31

Brief Summary

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Patients with dissection of the descending aorta will be followed up according to a precise timeline.

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Detailed Description

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NMR baseline A PET Scanner will be performed minimum 3 months post dissection 6 months and every year during three years after PET scanner : CT scanner and blood sample

Conditions

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Dissection of the Descending Aorta

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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TEP-18FDG for every patient after aortic dissection

Cover key details of the intervention. Must be sufficiently detailed to distinguish between arms of a study (e.g., comparison of different dosages of drug) and/or among similar interventions (e.g., comparison of multiple implantable cardiac defibrillators). For example, interventions involving drugs may include dosage form, dosage, frequency and duration.

Example: 50 mg/m2, IV (in the vein) on day 5 of each 28 day cycle. Number of Cycles: until progression or unacceptable toxicity develops.

Intervention Type RADIATION

Other Intervention Names

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TEP-18FDG

Eligibility Criteria

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Inclusion Criteria

* 18 years
* Seen for dissection of the descending aorta
* Dissection of the descending aorta within the last three months
* Affiliation to social security
* Signed informed consent