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Arterial Wave Energy Flux and Multidimensional Recovery in Patients With Chronic Thromboembolic Pulmonary Hypertension Undergoing Balloon Pulmonary Angioplasty

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Observational
SUMMARY

The goal of this observational study is to learn if advanced heart pressure wave analysis (called WIA and REPA) can help track and predict clinical improvement in adults (aged 18-85) with Chronic Thromboembolic Pulmonary Hypertension (CTEPH) who are undergoing Balloon Pulmonary Angioplasty (BPA). The main questions it aims to answer are: Do changes in these advanced heart pressure wave patterns relate to improvements in a patient's walking distance, heart function, and overall quality of life after BPA treatment? Are these new measurements more effective than standard heart pressure tests at showing how much a patient has truly improved? Participants will: Undergo standard Balloon Pulmonary Angioplasty (BPA) sessions as part of their regular medical care for CTEPH. Have their heart pressure waves recorded through a catheter during the routine BPA procedure (this does not require any extra surgical steps). Complete walking tests (6-minute walk test), blood tests, and heart ultrasounds (echocardiography) before starting the treatment and after it is completed. Fill out short surveys regarding their daily physical activity and quality of life.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• Age 18-85 years.

⁃ Confirmed diagnosis of CTEPH by a multidisciplinary CTEPH team and deemed eligible for BPA.

⁃ Hemodynamics compatible with pre-capillary PH according to current guidelines, as assessed by RHC (Right Heart Catheterization).

⁃ Technically inoperable CTEPH or persistent/recurrent PH following PEA (Pulmonary Endarterectomy).

⁃ Written informed consent.

Locations
Other Locations
Turkey
Istanbul Mehmet Akif Ersoy Educational and Training Hospital
RECRUITING
Istanbul
Contact Information
Primary
Umit Bulut, MD
umit.bulut@saglik.gov.tr
+90(212) 692 20 00
Backup
Ahmet Tas, MD PhD
ahmettas.cor@gmail.com
+90(212) 692 20 00
Time Frame
Start Date: 2026-03-10
Estimated Completion Date: 2028-05-01
Participants
Target number of participants: 70
Treatments
Patients with CTEPH
Sponsors
Leads: Istanbul Mehmet Akif Ersoy Educational and Training Hospital

This content was sourced from clinicaltrials.gov