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NCT07122518Recruiting

Post-Approval Study of PALMAZ MULLINS XD™ in Treating Pulmonary Artery Stenosis

Cordis US Corp.

Start Date

6/23/2026

Completion Date

6/1/2028

Summary

The purpose of the clinical investigation is to characterize clinical outcomes and to assess the real-world use of the commercial PALMAZ MULLINS XD™ Pulmonary Stent.

Detailed Description

The clinical study is a prospective, single-arm, multi-center, post-approval study of all consecutive subjects treated with the PALMAZ MULLINS XD™ Pulmonary Stent. The study will enroll a minimum of 35 subjects and a maximum of 75 subjects in up to 11 U.S sites or until the end of the 2-year enrollment period has been reached, whichever comes first. The study will collect the performance and safety data of the PALMAZ MULLINS XD™ Pulmonary Stent through time of hospital discharge.

Eligibility Criteria

Age Range: No minimum to No maximum

\- Subjects \*should\* meet criteria as per the list of indications/contraindications in the Instructions for Use, though all subjects treated with the PALMAZ MULLINS XD™ Pulmonary Stent will be considered eligible and enrolled.

Interventions

DEVICE

PALMAZ MULLINS XD™ Pulmonary Stent

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Conditions

Pulmonary Artery Stenosis

Locations

UC Davis Children's Hospital

Sacramento, California 95817

United States

Children's Healthcare of Atlanta

Atlanta, Georgia 30329

United States

Children's Hospital of Michigan

Detroit, Michigan 48201

United States

St Louis Children's Hospital

St Louis, Missouri 63110

United States

University of Nebraska Medical Center

Omaha, Nebraska 68114

United States

Children's Hospital Medical Center

Cincinnati, Ohio 45229

United States

UMPC Children's Hospital of Pittsburgh

Pittsburgh, Pennsylvania 15224

United States

Texas Children's Hospital

Houston, Texas 77030

United States