Comparison of EVAR and ESAR for Infrarenal Aortic Aneurysms With a Wide Proximal Neck
A legfontosabb adatok
- Hol
- Buffalo, Columbia, Detroit, Hershey, Kingsport, Maywood, Miami Beach, Minneapolis, New Brunswick, Raleigh, Richmond, Royal Oak, St Louis, Stony Brook, Toledo és Washington (Egyesült Államok)Mind a 16 helyszín megnézése
Helyszínek itt: Egyesült Államok
- Sisters of Charity HospitalBuffalo, Egyesült ÁllamokContact: P Anain, MD (principal investigator)Résztvevőt keres
- University of MissouriColumbia, Egyesült ÁllamokContact: T. Vogel, MD (principal investigator)Résztvevőt keres
- Henry Ford HospitalDetroit, Egyesült ÁllamokContact: Dr. Mitchel WeaverToborzás még nem indult
- Penn State Health Milton S. Hershey Medical CenterHershey, Egyesült ÁllamokContact: Dr. Faisal Aziz, MDRésztvevőt keres
- Ballad Health/Holston ValleyKingsport, Egyesült ÁllamokContact: R. Allen, MD (principal investigator)Résztvevőt keres
- LoyolaMaywood, Egyesült ÁllamokContact: P. Dr. Halandras, MDRésztvevőt keres
- Mt Sinai Med CtrMiami Beach, Egyesült ÁllamokContact: M Ayad, MD (principal investigator)Résztvevőt keres
- Alina HealthMinneapolis, Egyesült ÁllamokContact: J. Jim, MD (principal investigator)Résztvevőt keres
- Robert Wood Johnson University Medical CenterNew Brunswick, Egyesült ÁllamokContact: Beckerman, MD (principal investigator)Résztvevőt keres
- NC Heart& VascularRaleigh, Egyesült ÁllamokContact: R. Mendez, MD (principal investigator)Résztvevőt keres
- Virginia Commonwealth University (Vcu)Richmond, Egyesült ÁllamokContact: Newton, MD (principal investigator)Résztvevőt keres
- Beaumont University HospitalRoyal Oak, Egyesült ÁllamokContact: O.W. Brown, MD (principal investigator)Résztvevőt keres
- Barnes-Jewish HospitalSt Louis, Egyesült ÁllamokContact: L Sanchez, MD (principal investigator)Résztvevőt keres
- Stony Brook University Medical CenterStony Brook, Egyesült ÁllamokContact: A. Tassiopoulos, MD (principal investigator)Résztvevőt keres
- ProMedica Toledo HospitalToledo, Egyesült ÁllamokContact: B. Aplin, MD (principal investigator)Résztvevőt keres
- Washington Regional Medical CenterWashington, Egyesült ÁllamokContact: R. Wood, MD (principal investigator)Résztvevőt keres
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakA vizsgálat adatai
- Ki végzi
- Rijnstate Hospital
- Azonosító
- NCT05484115
- A regiszteradat frissítve
- 2026. május 11.
- Eredeti leírás
The HERCULES trial is a Randomized controlled clinical trial designed to prospectively compare endosuture aneurysm repair (ESAR) to standard endovascular aneurysm repair (EVAR) clinical outcomes in treatment of infrarenal abdominal aortic aneurysm (AAA) in subjects having wide proximal aortic neck diameters (≥ 28mm and ≤ 32mm).A teljes eredeti leírásKevesebb
Randomized Controlled Clinical Trial on the Application of Heli-FX EndoAnchors in Conjunction With the Endurant II/IIs Endograft in Infrarenal Aortic Aneurysms With a Wide Infrarenal Neck (HERCULES Trial)
The HERCULES trial is a Randomized controlled clinical trial designed to prospectively compare endosuture aneurysm repair (ESAR) to standard endovascular aneurysm repair (EVAR) clinical outcomes in treatment of infrarenal abdominal aortic aneurysm (AAA) in subjects having wide proximal aortic neck diameters (≥ 28mm and ≤ 32mm).
Bevonási feltételek: Age 18 years or older; Provided written informed consent; Clinical necessity for treatment of the AAA, according to the current guidelines in the geographies participating; Elective repair; Eligible anatomy for treatment with the Endurant II/IIs stent graft system and Heli-FX EndoAnchor system according to the IFU of both devices; Infrarenal neck diameter ≥ 28 mm and ≤32 mm; Proximal neck length ≥10mm.
Kizáró feltételek: Patient had a Cerebro Vascular Accident (CVA) or a myocardial infarction (MI) within the prior three months; Patient has active COVID-19 infection or has been diagnosed with long COVID-19 requiring hospitalization within the 6 months prior to procedure; Patient has previously been treated with stent grafts in the aorto-iliac arteries; Patient has a psychiatric or other condition that may interfere with the study; Patient has a known allergy to any device component; Patients with a systemic infection who may be at increased risk of endovascular graft infection; Patient has a coagulopathy or uncontrolled bleeding disorder; Patient with eGFR < 30 ml/min/1.73m2 before the intervention; Patient's life expectancy <2 years as judged by the investigator; Anatomy outside the IFU of the ndurant II/IIs stent graft system and Heli-FX EndoAnchor system; Planned use of AUI main body device; Patient is participating in another clinical study, potentially conflicting with the outcomes of the current study; Patient has a ruptured, leaking, or mycotic aneurysm; Patient is not eligible for standard EVAR; Patient is pregnant (Female patients of childbearing potential only).