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Patient Reported Side Effects of Pulmonary Hypertension (PH) Medications

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City:   Stanford
State:   California
Zip Code:   94305
Conditions:   Pulmonary Hypertension
Purpose:   The study seeks to analyze the patient reported effects of pulmonary hypertension medications and compare these with the side effects described on the package inserts. Side effects for these PH medications have been described in the adult population, but have never been described in the pediatric population. This information can better improve patient care and be used to characterize the side effects resultant from these medications.
Study Summary:   As part of standard of care, patients are routinely asked about any symptoms they might be experiencing. This study seeks to quantify these symptoms for research purposes. Participants will be identified through those who attend the pediatric pulmonary hypertension clinic at LPCH. Only children who are currently on one of seven PH medications (Bosentan, Epoprostenol, Letairis, Sildenafil, Tadalafil, Treprostinil, Ventaris) will be approached. Patients who consent to be in the study will answer a brief series of questions pertaining to the presence and duration of their symptoms. These will be correlated to a list of side effects taken from Lexicomp (a medication database).
Criteria:   Inclusion Criteria: - pulmonary hypertension - currently taking at least one of the following PH medications (Bosentan, Epoprostenol, Letairis, Sildenafil, Tadalafil, Treprostinil, Ventaris) Exclusion Criteria: - >18 years
NCT ID:   NCT01571713
Primary Contact:   Jeffrey Feinstein, MD, MPH
Phone: 650 723 7913
Email: jeff.feinstein@stanford.edu
Backup Contact:   N/A
Location Contact:   Stanford, California 94305
United States

Jeffrey Feinstein, MD, MPH
Phone: 650-723-7913
Email: jeff.feinstein@stanford.edu

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 18, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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