EndoSure Sensor for Long-term Follow-up After Endovascular AAA Repair (PRICELESS)
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ClinicalTrials.gov Identifier: NCT00831870
Verified August 2012 by CardioMEMS. Recruitment status was: Enrolling by invitation
The purpose of this study is to collect and compare EndoSure and EndoSure s2 Wireless AAA Pressure Sensor measurements with measurements from CT scan imaging, ultrasound, and other tests used to measure your AAA sac size and endoleaks following AAA repair, and during follow-up visits with your physician. An antenna is held over the patient's abdomen to measure pressure inside the aneurysm sac. The reading does not cause any discomfort, and dye or radiation is not needed to take the pressure measurement. To qualify, the patient must have a previously implanted EndoSure Sensor.
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Ages Eligible for Study:
18 Years and older (Adult, Senior)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Male or female subjects, at least 18 years of age, who are post-EndoSure AAA Pressure Sensor implantation at time of enrollment.
Written informed consent obtained from subject or legal guardian
Males or females, at least 18 years of age
Subjects who are post-EndoSure Wireless AAA Pressure Sensor implantation, with pressure measurements at implant.
Subjects willing to comply with the site-specific follow-up requirements of the investigator.
Subjects whose clinical condition, in the Investigator's opinion, would not allow them to complete participation in the registry.