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Cutting Balloon Study

NCT01205568 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 73

Last updated 2018-05-25

Study results available
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Summary

The primary objective of this study is to evaluate the safety and efficacy of transcatheter Cutting Balloon therapy for branch pulmonary artery stenosis resistant to low pressure dilation.

Conditions

  • Pulmonary Artery Stenosis

Interventions

DEVICE

Transcatheter Cutting Balloon therapy

PROCEDURE

High Pressure Balloon Angioplasty

Sponsors & Collaborators

Principal Investigators

  • Kathy Jenkins, MD, MPH · Boston Children's Hospital

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-08-01
Primary Completion
2009-03-17
Completion
2009-09-09

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

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 NCT01205568 on ClinicalTrials.gov