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

NCT06726928 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 78

Last updated 2025-09-04

No results posted yet for this study

Summary

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

Conditions

  • Treatment of Symptomatic Lateral Sinus Stenosis
  • Treatment of Pulsatile Tinnitus Due tu Sinus Stenosis

Interventions

DEVICE

Sinus Stenting

Stenting of symptomatic sinus stenosis

Sponsors & Collaborators

  • Acandis GmbH

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-09-30
Primary Completion
2027-01-31
Completion
2029-01-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06726928 on ClinicalTrials.gov