Detection of Pulmonary Embolism With CECT
Completed · Phase 4
Conditions studied: Pulmonary Embolism
In brief
To compare the vascular enhancement of the two contrast agents in pulmonary Multi-detector CTA
Key facts
- Study ID
- NCT00351754
- Run by
- Bracco Diagnostics, Inc
- People needed
- 120
- Starts
- 2006-07-01
- Expected to finish
- 2006-11-01
- Last updated by the study team
- 2008-01-07
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients 18 yrs or older
- With suspected PE
- Referred for MDCTA of pulmonary arteries
- Signed informed consent
You may not qualify if…
- Pregnant and lactating females
- History of hypersensitivity to iodinated contrast agents
- Hyperthyroidism or pheochromocytoma
- Severe CHF
- Renal impairment
- Weight greater than 300 lbs
- Pacemaker
- Swan Ganz catheter
- Defibrillator or other intrathoracic metallic vascular device
- Received an investigational compound within 30 days of being in the study
Where it is running
- Bracco Diagnostics, Inc. — Princeton, New Jersey, United States
Full record on ClinicalTrials.gov
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