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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06267573
Other study ID # Kerolos protocol
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date September 2024
Est. completion date September 10, 2026

Study information

Verified date February 2024
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Evaluation of the effectiveness of the different modalities for treatment of thoracoabdominal aortic aneurysms. FEVAR and BEVAR devices are widely used now due to its feasability and wide range of use . We aim to evaluate the effectiveness of these new devices in the management of TAAA


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date September 10, 2026
Est. primary completion date September 15, 2025
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - all adult consecutive patients presenting with TAAA larger than 5.5 cm Exclusion Criteria: - active infection Asymptomatic patients with small aneurysms Allergy to contrast agents

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Fenestrated and branched endovascular devices for TAAA
Devices for TAAA

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary Successful cannulation of the target vessels with complete in-line flow to target organs. No ischemia Two years
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