SiREX-Stent for the Treatment of SymptOmatic Lateral VEnous Sinus Stenosis

Recruiting N/A Interventional Study
Treatment of Symptomatic Lateral Sinus Stenosis Treatment of Pulsatile Tinnitus Due tu Sinus Stenosis
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
78 (estimated)
Sponsor
Acandis GmbH · Industry
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About This Trial

The purpose of the study is to assess the efficacy, safety and the clinical benefit of the SiREX stent for the treatment of disabling pulsatile tinnitus due to stenosis of lateral sinus. The study will enrol patients suffering from pulsatile tinnitus related to a lateral sinus stenosis lasting more than three months, and who want to be treated with lateral sinus stenting

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * • Patient ≥ 18 years old * Disabling pulsatile tinnitus lasting for more than three months * Venous type: pulsatile tinnitus is interrupted by ipsilateral jugular vein compression * Lateral sinus stenosis visible on venous MRA or venous angio CT * Exclusion of other c…
Contacts

Anna Gold

+49 7231 155000

info@acandis.com

CONTACT