Imaging of Dissection of the Descending Aorta (DADI)

This study is currently recruiting participants. (see Contacts and Locations)
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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

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 July 24, 2014