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International BPA Registry

NCT03245268 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2022-06-10

No results posted yet for this study

Summary

The International Balloon Pulmonary Angioplasty (BPA) Registry is a prospective, multi-center, long-term observational project. Scheduled to start data collection in Q4 2017, the registry will run for approximately four years with a follow-up time for each patient of at least two years. Its primary objective is to investigate the efficacy and safety of BPA intervention in patients with chronic thromboembolic pulmonary hypertension (CTEPH) not amenable to pulmonary endarterectomy (PEA).

Conditions

  • Chronic Thromboembolic Pulmonary Hypertension
  • CTEPH

Interventions

PROCEDURE

Balloon pulmonary angioplasty

BPA is an interventional technique where a balloon catheter is used to recanalize affected segments of pulmonary arteries identified during angiography.

Sponsors & Collaborators

  • International CTEPH Association

    lead OTHER

Principal Investigators

  • Nick H Kim, Prof · International CTEPH Association

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-03-02
Primary Completion
2022-03-31
Completion
2022-03-31

Countries

  • United States
  • Austria
  • Belgium
  • Czechia
  • France
  • Germany
  • Japan
  • Netherlands
  • Poland
  • United Kingdom

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 NCT03245268 on ClinicalTrials.gov