Extracranial Carotid Artery Aneurysm Clinical Trial
Official title:
Extracranial Carotid Artery Aneurysm Registry
To prospectively collect data on ECAA we designed the Carotid Aneurysm Registry (CAR). The aim of this study is to collect data on ECAA and its treatment to assess the natural history of ECAA and the success and safety of different treatment strategies.
CAR is a prospective observational study, initiated by the Department of Vascular Surgery at
University Medical Centre Utrecht (UMCU), The Netherlands. The study is descriptive in
nature. The registry will be conducted according to the principles of the Declaration of
Helsinki (64th WMA General Assembly, Fortaleza, Brazil, October 2013). The medical ethics
committee of the UMCU has approved the study and all patients must give written informed
consent before enrollment. Study enrolment is open to any patient diagnosed with an ECAA and
ongoing.
Enrollment criteria: Participation in the CAR is intended for all subjects diagnosed with an
ECAA irrespective of chosen treatment. Aneurysms are defined as 150% dilatation of the
normal vessel diameter, or any saccular aneurysm. To be included, aneurysms must be located
in the CCA, the external carotid artery or in the extracranial part of the ICA.To be
included in the registry, patients need to be 18 years old. There are no additional
exclusion criteria.
Intervention and follow-up:CAR does not interfere with the physician's treatment decision.
Follow-up visits and imaging studies are scheduled as usual in their clinical practice, as
this study does also not interfere with or influence the follow-up regimen.
Study endpoints:The primary endpoint of the CAR is freedom from aneurysm related symptoms at
30 days and at mid- and longterm follow-up. The secondary endpoint comprises treatment
safety.
Endpoint monitoring:An endpoint adjudication committee, consisting of clinical experts, is
set up to harmonize and standardize endpoint assessment and to determine whether the
endpoints meet described criteria. This committee will review important subjective endpoints
reported by trial investigators. The members of this committee are blinded to the treatment
regime.
Data collection and monitoring: Data collected will be recorded through a web-based case
report form (CRF). Data will be collected at baseline, at the moment of intervention, at the
30-day (or first postoperative) visit and during the follow-up phase. Data will remain at
the UMCU in a secure environment.
This registry is a multicenter study. Statistical analysis: Statistical analyses will be
performed using SPSS software.
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Observational Model: Cohort, Time Perspective: Prospective
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT05828576 -
ECAA Brain MRI: Seeking the Link Between Extracranial Carotid Artery Aneurysms and Small Vessel Disease
|