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The BLIMP Balloon in Coronary Interventions

NCT03947398 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 128

Last updated 2023-01-27

No results posted yet for this study

Summary

The purpose of this study is to investigate the effectivness of the Blimp Scoring balloon compared to current available CTO balloon catheters.

Conditions

  • Percutaneous Coronary Intervention
  • Chronic Total Occlusion of Coronary Artery

Interventions

DEVICE

BLIMP balloon

Using BLIMP balloon to cross lesion

DEVICE

Low profile balloon

using low profile balloon to cross lesion

Sponsors & Collaborators

  • Ziekenhuis Oost-Limburg

    collaborator OTHER

  • AZ Sint-Jan AV

    collaborator OTHER

  • CHU de Charleroi

    collaborator OTHER

  • Jolimont, La Louviere

    collaborator UNKNOWN

  • Centre Hospitalier Universitaire Saint Pierre

    collaborator OTHER

  • Onze Lieve Vrouwziekenhuis Aalst

    collaborator OTHER

  • Centre Hospitalier Universitaire UCLouvain Namur

    collaborator OTHER

  • University Ghent

    collaborator OTHER

  • University Hospital, Antwerp

    collaborator OTHER

  • Centre Hospitalier du Luxembourg

    collaborator OTHER

  • Universitaire Ziekenhuizen KU Leuven

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-03-28
Primary Completion
2021-03-28
Completion
2021-03-28

Countries

  • Belgium

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 NCT03947398 on ClinicalTrials.gov