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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT01648933
Date of registration: 12/04/2012
Prospective Registration: Yes
Primary sponsor: Assistance Publique - Hôpitaux de Paris
Public title: Perfusion Analysis Using Rubidium in Cardiac Sarcoidosis PARCS
Scientific title: Perfusion Analysis Using Rubidium in Cardiac Sarcoidosis
Date of first enrolment: July 2012
Target sample size: 53
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT01648933
Study type:  Interventional
Study design:  Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Diagnostic. Masking: None (Open Label).  
Phase:  N/A
Countries of recruitment
France
Contacts
Name:     Dominique Le Guludec, MD, PhD
Address: 
Telephone:
Email:
Affiliation:  Assistance Publique - Hôpitaux de Paris
Key inclusion & exclusion criteria

Inclusion Criteria:

- (1) histologically proven sarcoidosis;

- (2) suspicion of cardiac involvement on symptoms, and/or ECG and/or echocardiogram.

Exclusion Criteria:

- patient < 18 years old



Age minimum: 18 Years
Age maximum: N/A
Gender: All
Health Condition(s) or Problem(s) studied
Sarcoidosis
Intervention(s)
Radiation: Rubidium PET
Primary Outcome(s)
percentage of patient who has two different diagnostic and therapeutic attitude before knowing Rubidium-82 PET result and after knowing Rubidium-82 PET result [Time Frame: 60 days]
Secondary Outcome(s)
Analysis of the cost for the use of Sestamibi SPECT and Rb-PET as MPI agents in cardiac sarcoidosis. [Time Frame: 9 months]
Secondary ID(s)
AOR10027
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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