Clinical Study of Aneurysm Exclusion
Status unconfirmed · Phase 1
Conditions studied: Aneurysm
In brief
The ultimate purpose is to explore potential techniques to exclude aneurysms and provide alternative conduit for arterial flow. The single center sponsorship is intended to provide the investigators the potential to incorporate improvements in existing technology during the course of the study thereby ultimately enhancing the potential for superior medical care of patients suffering from these disease states.
Key facts
- Study ID
- NCT00549380
- Run by
- Arizona Heart Institute
- People needed
- 88
- Starts
- 1999-10-01
- Expected to finish
- 2010-10-01
- Last updated by the study team
- 2010-05-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- ≥ 18 years old
- Informed consent understood and signed.
- Compliance with post-treatment follow-up requirements.
- Candidates in this study may not be ideal surgical patients and therefore may be included based upon the recommendation of the principal investigator or co-investigators and one independent consultant confirming the opinion of the investigators.
- Patient may present as an emergency or urgent use patient with indications including: ruptured aneurysm, dissected artery, or transected artery.
You may not qualify if…
- Life expectancy < 2 years.
- Pregnant or lactating women.
- Indication that appropriate follow-up studies would for whatever reason be difficult to obtain.
- Patient has other medical or psychiatric problems, which in the opinion of the investigator, precludes them from participating in the study.
- Anticoagulation drugs are indicated.
- Coagulopathy or bleeding disorder.
- Active systemic or localized groin infection.
- Inferior mesenteric artery is indispensable.
- Creatinine level > 1.7 mg/dl.
Where it is running
- Arizona Heart Institute — Phoenix, Arizona, United States
Full record on ClinicalTrials.gov
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