WithdrawnNCT03833323
Implantable System for Remodulin Post-Approval Study
Studying Drug- or toxin-induced pulmonary arterial hypertension
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Medtronic Cardiac Rhythm and Heart Failure
- Principal Investigator
- Robert Bourge, MDUniversity of Alabama at Birmingham
- Intervention
- Implantable System for Remodulin (treprostinil)(combination_product)
- Eligibility
- 22 years · All sexes
- Timeline
- 2020 – 2021
Collaborators
United Therapeutics
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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