Actively Recruiting

Age: 18Years +
All Genders
NCT06607731

Percutaneous Gelled Alcohol Sclerotherapy for Aggressive Angiomas: Evaluation of Feasibility, Safety, and Efficacy

Led by Centre Hospitalier Universitaire de Saint Etienne · Updated on 2024-10-08

11

Participants Needed

1

Research Sites

22 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The investigators aimed to evaluate efficacy and safety of a non-surgical protocol treatment combining transarterial embolization and percutaneous radiopaque gelled ethanol (RGE) sclerotherapy in a first procedure, then followed by vertebroplasty in a second procedure, to treat aggressive vertebral hemangioma patients in tertiary hospital. Exclusion criteria were age \<18-years old and any association with neurological deficit.

CONDITIONS

Official Title

Percutaneous Gelled Alcohol Sclerotherapy for Aggressive Angiomas: Evaluation of Feasibility, Safety, and Efficacy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients treated by gelled alcohol sclerotherapy for aggressive angiomas at the University Hospital of Saint-Etienne
Not Eligible

You will not qualify if you...

  • Patients not treated by gelled alcohol sclerotherapy
  • Age under 18 years
  • Presence of any neurological deficit

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
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3
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Trial Site Locations

Total: 1 location

1

CHU de Saint-Etienne

Saint-Priest-en-Jarez, France, 42270

Actively Recruiting

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Research Team

S

Sylvain GRANGE, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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