Actively Recruiting

Age: 18Years - 99Years
All Genders
NCT05916898

The Lower Silesia Shockwave Registry

Led by Regional Cardiology Center, The Copper Health Centre (MCZ), · Updated on 2023-06-23

400

Participants Needed

2

Research Sites

260 weeks

Total Duration

On this page

Sponsors

R

Regional Cardiology Center, The Copper Health Centre (MCZ),

Lead Sponsor

P

Provincial Specialized Hospital in Legnica

Collaborating Sponsor

AI-Summary

What this Trial Is About

Lower Silesia Shockwave Registry (LSSR), is a observational registry collecting all consecutive cases of percutaneous coronary intervention (PCI) performed with the support of shockwave intravascular lithotripsy in two cooperating cardiac centers (Department of Cardiology, The Copper Health Centre, Lubin Poland, and Department of Cardiology, Provincial Specialized Hospital in Legnica, Poland).

CONDITIONS

Official Title

The Lower Silesia Shockwave Registry

Who Can Participate

Age: 18Years - 99Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Presence of moderately to severely calcified coronary artery lesions
  • Significant under-expansion (greater than 20% diameter) of a previously implanted stent
  • Initial unsuccessful lesion preparation with non-compliant balloon catheter or atherectomy device
Not Eligible

You will not qualify if you...

  • Lack of patient consent
  • Target vessel dissection type 3 or higher (SCAD classification)
  • Target vessel perforation from previous unsuccessful lesion preparation
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Department of Cardiology, Provincial Specialized Hospital in Legnica,

Legnica, Lower Silesian Voivodeship, Poland, 59-220

Actively Recruiting

2

Department of Cardiology, The Copper Health Centre (MCZ)

Lubin, Lower Silesian Voivodeship, Poland, 59-300

Actively Recruiting

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Research Team

A

Adrian Włodarczak, M.D; Ph. D; Assoc Prof.

CONTACT

P

Piotr Rola, M.D.; Ph.D.

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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