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Aortic Aneurysm, Abdominal clinical trials

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NCT ID: NCT00646048 Completed - Clinical trials for Abdominal Aortic Aneurysm

A Phase I Evaluation of the Safety of the TriVascular Stent-Graft System in the Treatment of Abdominal Aortic Aneurysms

AAA IDE
Start date: February 2003
Phase: Phase 1
Study type: Interventional

This study was a prospective observational study examined the safety of the TriVascular AAA Stent-Graft System in the elective treatment of patients with abdominal aortic aneurysms. Specifically, the study will evaluate the safety of the TriVascualr AAA Stent-Graft System, evaluate the ability to deliver the Tri-Vascular AAA Stent-Graft System to the desired location within the aorta, and evaluate the ability of the TriVascular AAA Stent-Graft to exclude the abdominal aortic aneurysm.

NCT ID: NCT00615069 Completed - Clinical trials for Aortic Aneurysm, Abdominal

Study of the Large Diameter GORE EXCLUDER® AAA Endoprosthesis in Abdominal Aneurysms

Start date: May 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of the 31 mm GORE EXCLUDER® AAA Endoprosthesis in the treatment of infrarenal abdominal aortic aneurysms

NCT ID: NCT00612924 Completed - Clinical trials for Infrarenal Abdominal Aortic Aneurysm

The Vascutek AnacondaTM Stent Graft System Phase II IDE Study

Start date: April 2009
Phase: N/A
Study type: Interventional

The Phase I safety study is now complete. FDA approval has been granted to proceed to Phase II. The primary objectives of the Phase II study is to assess the safety and effectiveness of the Anaconda Stent Graft System in subjects presenting with abdominal aortic aneurysm (AAA). The secondary objectives of this study are to assess additional clinical outcomes measurements associated with treatment of AAA using the Anaconda Stent Graft System

NCT ID: NCT00610090 Terminated - Clinical trials for Abdominal Aortic Aneurysms

Safety Study for the Treatment of Abdominal Aortic Aneurysms

UNITE
Start date: May 2007
Phase: Phase 2
Study type: Interventional

The primary study objective, at this time, is to follow out to 5 years post implant the safety of already enrolled subjects who were treated with the UniFit Aorto-uni-iliac (AUI) Endoluminal Stent Graft (the "study device") for the repair of abdominal aortic aneurysms (AAAs).

NCT ID: NCT00604643 No longer available - Clinical trials for Abdominal Aortic Aneurysms

Talent Aortic Cuff Stent Graft System Compassionate Use Registry

Start date: n/a
Phase:
Study type: Expanded Access

An evaluation of the TALENT Aortic Cuff in patients with existing AneuRx stent grafts who have experienced sub-optimal stent graft outcomes and are not deemed suitable candidates for treatment with an AneuRx Aortic Cuff.

NCT ID: NCT00604552 Terminated - Abdominal Aneurysm Clinical Trials

AneuRx Post Market Study in the Treatment of AAA

Start date: July 2003
Phase: N/A
Study type: Interventional

The aorta is a large blood vessel that carries blood away from the heart to the organs in the rest of the body. An aneurysm is a weakening in the artery wall that will become a bulge in the aorta. If left untreated, this bulge may continue to grow larger and may rupture (break open) with fatal consequences. Abdominal aortic aneurysm (AAA) is a life-threatening lesion that has been treated in recent year via endovascular repair. The purpose of this study is to monitor the long term performance of the AneuRx Stent Graft Systems.

NCT ID: NCT00593814 Completed - Clinical trials for Aortic Aneurysm, Abdominal

GORE EXCLUDER® Endoprosthesis - Low Permeability in Treatment of Abdominal Aortic Aneurysms

Start date: June 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the performance of the GORE EXCLUDER® Bifurcated Endoprosthesis-Low Permeability in the primary treatment of infrarenal abdominal aortic aneurysms.

NCT ID: NCT00591968 Completed - Clinical trials for Abdominal Aortic Aneurysm

Telesonography Adaptation and Use to Improve the Standard of Patient Care Within a Dominican Community

Start date: January 2008
Phase: N/A
Study type: Interventional

The role of teleradiology has far reaching implications for the health of remote and underserved populations. The ability to coordinate radiographic evaluation and diagnosis from a distance has the potential to raise the standard of patient care throughout the world. Perhaps the safest and most cost effective mode of teleradiology today is telesonography. The current project attempts to determine the extent that telesonography improves the standard of care within a rural government-run primary clinic within the Dominican Republic. The work reported herein is intended to compare the use of telesonography to the current standard of sonographic examination (referral to government hospital 60km from target clinic). The study was conducted by randomly assigning 100 patients with clinical indications for sonographic examination into experimental and control groups. Following a 60-day implementation period, the following research questions will be addressed: 1) To what extent does the use of asynchronous telesonography increase the percentage of definitive diagnoses based on the total number of scans (definitive diagnoses / total number of scans)? 2) To what extent does the use of asynchronous telesonography increase the continuity of care for patients? 3) To what extent does the elapsed time between scanning and final radiological interpretation decrease with the use of asynchronous telesonography? This study will also look at the history of telemedicine / telesonography and its dissemination into the mainstream practice of medicine, explore training protocols that may be used to assist others to establish new telesonography programs in a developing nations, and discuss both advances and persistent barriers to the implementation of telesonography programs. Hypothesis: The use of a store-and-forward telesonography system in this setting will increase the speed and number of final diagnoses per scan received by the target clinic and will increase the continuity of care by increasing the number and speed of follow-up appointments to the target clinic.

NCT ID: NCT00587977 Completed - Clinical trials for Abdominal Aortic Aneurysm

Aortic Distensibility

FAMRI
Start date: November 2004
Phase: N/A
Study type: Observational

Can software be developed to automatically aid in the measurement of abdominal aortic aneurysms, and is there a way to predict future rupture or growth of abdominal aortic aneurysms.

NCT ID: NCT00583414 Completed - Clinical trials for Abdominal Aortic Aneurysm

Endovascular Exclusion of Abdominal Aortic Aneurysms in High Risk Patients

Start date: September 1998
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the role of abdominal aneurysm and iliac aneurysm exclusion using an endovascular prosthesis.