Actively Recruiting
AIRDROP: Can we Improve Adherence to Inhaled Treatment for Pulmonary Arterial Hypertension?
Led by University of Sao Paulo General Hospital · Updated on 2026-03-09
72
Participants Needed
1
Research Sites
86 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Pulmonary Arterial Hypertension is a rare and progressive condition that compromises pulmonary circulation and can lead to right ventricular failure. Despite recent advances in diagnosis and treatment, the median survival of patients is only 2.8 years. The treatment for this disease is based on drugs that act on three main pathways: prostacyclin, endothelin, and nitric oxide. Iloprost, a prostacyclin analogue available in an inhaled form, is an important and well-established treatment. However, its mandatory frequent administration, the need for a specific inhalation technique, and its adverse event profile make its use complex. Although pharmacotherapeutic and inhalation technique follow-up by a qualified professional is widely studied in diseases like asthma and COPD, its application in Pulmonary Arterial Hypertension still lacks evidence. Thus, this study aims to evaluate how a pharmacist's intervention can improve treatment adherence, mitigate side effects and difficulties associated with inhalation, in addition to optimizing clinical and hemodynamic outcomes in patients with Pulmonary Arterial Hypertension using iloprost.
CONDITIONS
Official Title
AIRDROP: Can we Improve Adherence to Inhaled Treatment for Pulmonary Arterial Hypertension?
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients aged 18 years
- Treated at the referral center for PH management at the Heart Institute of the University of S�e3o Paulo Medical School
- Invasive confirmed diagnosis of Pulmonary Arterial Hypertension with mean pulmonary arterial pressure greater than 20 mmHg at rest
- Pulmonary vascular resistance equal to or greater than 2 Wood units
- Pulmonary capillary wedge pressure equal to or less than 15 mmHg
- Currently using iloprost inhaled treatment
You will not qualify if you...
- Unable to perform the 6-minute walk test (6MWT)
- Experienced gastrointestinal bleeding within the 12 weeks prior to the study start
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Incor HCFMUSP
São Paulo, São Paulo, Brazil, 01246-000
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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