Imaging of Dissection of the Descending Aorta (DADI)

This study is currently recruiting participants.
Verified July 2012 by Assistance Publique - Hôpitaux de Paris
Sponsor:
Collaborator:
Institut National de la Santé Et de la Recherche Médicale, France
Information provided by (Responsible Party):
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT01648881
First received: July 20, 2012
Last updated: January 29, 2014
Last verified: July 2012
  Purpose

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


Condition Intervention
Dissection of the Descending Aorta
Radiation: TEP-18FDG for every patient after aortic dissection

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Dissection of Aorta: Descending Part, Imaging

Resource links provided by NLM:


Further study details as provided by Assistance Publique - Hôpitaux de Paris:

Estimated Enrollment: 62
Study Start Date: May 2011
Estimated Study Completion Date: January 2018
Estimated Primary Completion Date: November 2016 (Final data collection date for primary outcome measure)
Intervention Details:
    Radiation: 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.

    Other Name: TEP-18FDG
Detailed Description:

NMR baseline after 3 months, after 6 months, and every year CT Scanner at baseline and after 3 months A PET Scanner will be performed at 3 months

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Patients with dissection of the descending aorta

Criteria

Inclusion Criteria:

  • 18 years
  • Seen for dissection of the descending aorta
  • Signed informed consent

Exclusion Criteria:

  • Pregnant female
  • Adults without legal capacity
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01648881

Contacts
Contact: Guillaume JONDEAU + 33 (0) 1 4025 68 11 guillaume.jondeau@bch.aphp.fr
Contact: Laurent MD LEPAGE laurent.lepage@bch.aphp.fr

Locations
France
Pr Guillaume JONDEAU . Cardiologie. Hôpital Bichat Recruiting
Paris, Ile de France, France, 75018
Contact: Guillaume JONDEAU    + 33 (0)140256811    guillaume.jondeau@bch.aphp.fr   
Sponsors and Collaborators
Assistance Publique - Hôpitaux de Paris
Institut National de la Santé Et de la Recherche Médicale, France
Investigators
Principal Investigator: Guillaume JONDEAU Assistance Publique - Hôpitaux de Paris
  More Information

No publications provided

Responsible Party: Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier: NCT01648881     History of Changes
Other Study ID Numbers: P 100505, 2011-A00238-33
Study First Received: July 20, 2012
Last Updated: January 29, 2014
Health Authority: France: Ministry of Health

ClinicalTrials.gov processed this record on April 16, 2014