Pararenal Aneurysm

4

Review clinical trials related to Pararenal Aneurysm. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Zenith® Fenestrated+ Clinical Study

The Zenith® Fenestrated+ Endovascular Graft Clinical Study will assess the safety and effectiveness of the Zenith® Fenestrated+ Endovascular Graft (ZFEN+) in combination with the BeGraft Balloon-Expandable FEVAR Bridging Stent Graft System (BeGraft) and Unibody2 for the treatment of patients with aortic aneurysms involving one or more of the major visceral arteries. Up to 60 additional subjects may be enrolled in Continued Access phase of the study

Participants needed: 105
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Cook Research IncorporatedUpdated: Mar 23, 2026Locations: 33
Eligibility criteria

Thoracoabdominal, pararenal or juxtarenal aortic aneurysm with a diameter ≥ 55 m... [+2]

Age < 18 years [+5]

Status: Recruiting

Clinical Outcomes and Major Adverse Events in Patients Treated With Physician-Modified Fenestrated and Branched Stent Grafts

The purpose of this study is to evaluate safety and effectiveness of endovascular treatment of juxtarenal, pararenal and thoracoabdominal aortic aneurysms (with or without iliac artery involvement) using physician-modified stent grafts with a combination of fenestrations and/or branches.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of California, Los AngelesUpdated: Dec 15, 2025Locations: 1
Eligibility criteria

Older than 75 years of age [+20]

Less than 18 years of age [+20]

Status: Recruiting

Frailty and Physician Modified Fenestrated Endograft for Thoracoabdominal Aortic Pathologies

The primary objective of this single arm, prospective feasibility study, Impact of Frailty on Clinical Outcomes of Patients Treated for Thoracoabdominal and Complex Abdominal Aortic Aneurysms with Physician-Modified Fenestrated and Branched Stent Grafts, is to assess the use of the physician-modified fenestrated/branched endografts to repair thoracoabdominal and complex aortic aneurysms in subjects having appropriate anatomy, at high risks for open repairs. The primary intent of the study is to assess safety and preliminary effectiveness of the device acutely (i.e., treatment success and technical success), at 30 days (i.e., the rate of major adverse events (MAE)) and at 3 months, 6 months, 12 months, and annually to 5 years (i.e., the proportion of treatment group subjects that achieve and maintain treatment success). Additionally, this study will assess the degree of patient frailty before and after the aneurysm repair, as well as the association between the preoperative baseline frailty and clinical outcomes detailed above. This will help improve subject selection in identification of high risk patients who would not only suffer poor clinical outcomes, but also experience decline in their functional status.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of Southern CaliforniaUpdated: Jul 1, 2024Locations: 1
Eligibility criteria

Patients may be included in the study if the patient has at least one of the fol... [+5]

Less than 18 years of age. [+7]

Status: Not yet recruiting

Safety and Effectiveness of Surgeon-Modified Stent Grafts forTreatment of Complex Aortic Aneurysms

The primary objective of the present study is to evaluate the safety, effectiveness, and clinical outcomes of surgeon-modified fenestrated stent grafts used to treat patients with failed previous infrarenal repairs (failed EVAR) and complex aortic aneurysms (thoracoabdominal, juxtarenal, pararenal, and paravisceral aneurysms).

Participants needed: 25
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Jesse Manunga, MDUpdated: Oct 6, 2022Locations: 1
Eligibility criteria

Age: ≥ 18 years old [+10]

Age: < 18 years old [+34]