This trial is active, not recruiting.

Condition dissection of the descending aorta
Treatment tep-18fdg for every patient after aortic dissection
Sponsor Assistance Publique - Hôpitaux de Paris
Collaborator Institut National de la Santé Et de la Recherche Médicale, France
Start date May 2011
End date December 2015
Trial size 89 participants
Trial identifier NCT01648881, 2011-A00238-33, P 100505


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

United States No locations recruiting
Other countries No locations recruiting

Study Design

Observational model cohort
Time perspective prospective

Eligibility Criteria

Male or female participants at least 18 years old.

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 Exclusion Criteria: - intervention programmed in relation with dissection of the descending aorta - Pregnant female - Adults without legal capacity

Additional Information

Official title Dissection of Aorta: Descending Part, Imaging
Principal investigator Guillaume JONDEAU
Description 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
Trial information was received from ClinicalTrials.gov and was last updated in December 2016.
Information provided to ClinicalTrials.gov by Assistance Publique - Hôpitaux de Paris.