fEVAR / bEVAR - Data Capture on Disease Process and Therapy of Intraabdominal Aortic Diseases

fEVAR / bEVAR - Data Capture on Disease Process and Therapy of Intraabdominal Aortic Diseases - fEVAR / bEVAR

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00015920

Enrollment

100

Registered

2019-09-05

Start date

2018-08-21

Completion date

Unknown

Last updated

2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

I71.0

Interventions

Group 1: Prospective - rgistration - data aquisition - follow Up of patients with branched and fenestrated EVAR procedures

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: age > 18, possible patient consent

Exclusion criteria

Exclusion criteria: refusal of patient consent, study cancellation

Design outcomes

Primary

Measure	Time frame
Clinical data collection of patient and procedure characteristics of thoracoabdominal aortic interventions demanding fenestrated and branched stent graft Solutions to maintain blood flow to renal and visceral arteries. Data collection includes age, sex, comorbidities and medication as well as stent graft type, procedure related material and technical intervention data. Perioperative and postoperative complications will be registered to evaluate treatment success. These include clinical outcome, postoperative complications and reinterventions. Follow Up data will be associated with Treatment characteristics and interventions quality control. Patient specific Treatment options should be controlled and evaluated with these criteria to optimize these personalized interventions. Other important effects include prediction of individual risk factors for complications and optimized selection of reintervention possibilities.	—

Measure

Time frame

Clinical data collection of patient and procedure characteristics of thoracoabdominal aortic interventions demanding fenestrated and branched stent graft Solutions to maintain blood flow to renal and visceral arteries. Data collection includes age, sex, comorbidities and medication as well as stent graft type, procedure related material and technical intervention data. Perioperative and postoperative complications will be registered to evaluate treatment success. These include clinical outcome, postoperative complications and reinterventions. Follow Up data will be associated with Treatment characteristics and interventions quality control. Patient specific Treatment options should be controlled and evaluated with these criteria to optimize these personalized interventions. Other important effects include prediction of individual risk factors for complications and optimized selection of reintervention possibilities.

—

Secondary

Measure	Time frame
Quality control, optimization of endovascular interventions	—

Countries

Germany

Contacts

Public ContactPhilipp Erhart

Klinik für Gefäßchirurgie und Endovaskuläre Chirurgie, Universitätsklinikum Heidelberg

philipp.erhart@med.uni-heidelberg.de06221 56 36668

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Apr 4, 2026