Switching Sildenafil to Riociguat in Chronic Thromboembolic Pulmonary Hypertension After Balloon Pulmonary Angioplasty

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

This study was designed to investigate the safety and efficacy of replacing phosphodiesterase 5 inhibitors (PDE5i) with riociguat in patients with Chronic thromboembolic pulmonary hypertension (CTEPH) who have undergone pulmonary angioplasty (BPA) and remains symptomatic despite treatments with PDE5i.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients with established diagnosis of CTEPH who are symptomatic after Balloon pulmonary angioplasty (BPA)

• Patients who are on stable maximally tolerated dose of sildenafil for at least 6 weeks as monotherapy, or in combination with other pulmonary hypertension specific therapies

• WHO functional class III at screening

• Stable dose of diuretics (if used) for at least 30 days at screening

• No recent hospitalisation due to pulmonary hypertension or heart failure for at least 30 days

Locations
Other Locations
Hong Kong Special Administrative Region
Prince of Wales Hospital
RECRUITING
Hong Kong
Contact Information
Primary
Daniel Xu Nurse
danielxu@cuhk.edu.hk
+85235051518
Time Frame
Start Date: 2024-07-25
Estimated Completion Date: 2027-01-22
Participants
Target number of participants: 30
Treatments
Other: Patients with Chronic Thromboembolic Pulmonary Hypertension
Patients with Chronic Thromboembolic Pulmonary Hypertension under Sildenafil treatment
Sponsors
Leads: Chinese University of Hong Kong

This content was sourced from clinicaltrials.gov