Balloon Pulmonary anGiOplasty Versus Pulmonary Endarterectomy in Patients With Chronic ThromboEmbolic Pulmonary Hypertension: a Non-inferiority Randomized Trial

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Chronic thromboembolic pulmonary hypertension (CTEPH) is a rare and potentially life-threatening progressive disease that evolves from unresolved pulmonary embolism. Gold standard treatment for CTEPH is pulmonary endarterectomy (PEA) performed by skilled cardio-thoracic surgeons. Some patients may not be surgical candidates due to co-morbidities or because the vascular lesions are too distal making them technically inoperable. In these patients, balloon pulmonary angioplasty (BPA) has emerged as an effective treatment. In a subgroup of patients, the distribution of vascular lesions makes it possible to perform either BPA or PEA. There has never been a head-to head comparison of BPA with PEA. The aim of this study is therefore, to evaluate if BPA is non-inferior to PEA in patients with (CTEPH) who are eligible for both treatments.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 79
Healthy Volunteers: f
View:

• Diagnosed with chronic thromboembolic pulmonary hypertension according to current European society of cardiology/European Respiratory Society guidelines and eligible for both pulmonary endarterectomy and ballon pulmonary angioplasty by decision at the local multidisciplinary team conference and central adjudication committee

• Written informed consent from the patient

• Patient age \>17 and \<80 years

• Able to understand and follow instructions and to participate in the entire study period

Locations
Other Locations
Denmark
Aarhus University Hospital
RECRUITING
Aarhus
United Kingdom
Royal Ppworth
RECRUITING
Cambridge
Contact Information
Primary
Asger Andersen, MD, ass.prof.
asger.andersen@clin.au.dk
40138052
Backup
Kristina Laut Matzen, RN,PhD
krlaut@clin.au.dk
+4521673903
Time Frame
Start Date: 2024-04-01
Estimated Completion Date: 2028-04-01
Participants
Target number of participants: 139
Treatments
Active_comparator: BPA group
Balloon pulmonary angioplasty. Typically 4-8 sessions are needed to treat the patient. The specific pre-planning protocol, choice of wires and balloons, the number of vessels treated per session, and the decision that no further BPA sessions are needed is at the discretion of the treating physician.
Active_comparator: PEA group
Patients randomized to PEA will undergo surgery within 4 months after randomization and optional run-in phase. Distality of the dissection plane is at the discretion of the operating physicians.
Sponsors
Collaborators: Medical University of Vienna, Amsterdam UMC, location VUmc, St. Antonius Hospital, Kerckhoff Klinik, KU Leuven, Utrecht University, Papworth Hospital NHS Foundation Trust
Leads: University of Aarhus

This content was sourced from clinicaltrials.gov