Functional imaging after carotid endarterectomy for detection of cerebral hyperperfusion syndrome

Not Applicable

• Conditions: cerebral hyperfusion syndrome after carotid revascularization, measurement of cerebral blood volume; I67.9; Cerebrovascular disease, unspecified

• Registration Number: DRKS00026653
• Lead Sponsor: Siemens Healthcare GmbH

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2017-12-31
• Study Start: 2021-09-27
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 45

Inclusion Criteria

unilateral carotid stenosis

Exclusion Criteria

Patients with contralateral stenosis of >50%, patients with acute or chronic renal failure, as well as patients with intolerance to contrast medium were excluded.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
perioperative change in CBV measurements

Secondary Outcome Measures

Name	Time	Method
periprocedural stroke, TIA, postoperative CHS, and perioperative mortality and morbidity including postoperative hypertension