Tyvaso Dosing and Titration Evaluation: TyTRATE Registry

Completed

Conditions studied: Pulmonary Arterial Hypertension

In brief

This prospective, observational, multi-center, patient registry will follow patients who are newly initiated on Tyvaso for the treatment of Pulmonary Arterial Hypertension (PAH). Once enrolled, the patients' dose and titration will be followed for the first 6 months of treatment with Tyvaso. A call-center will contact the patients directly at weeks 1, 2, 3, 4, 8, 12, 16, 20, and 24 to review their dose and titration schedule. In addition to patient-reported dosing data, some patient demographic information, will be collected by the investigative site at Baseline.

Key facts

Study ID
NCT01799473
Run by
United Therapeutics
People needed
98
Starts
2013-01-01
Expected to finish
2014-12-01
Last updated by the study team
2015-03-24

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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