TrEatment Approach in the Multimodal Era Registry
NCT05629052 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000
Last updated 2025-05-08
Summary
The goal of this observational patient registry is to learn how expert centers treat patients with chronic thromboembolic pulmonary hypertension (CTEPH). CTEPH is a condition in which blood clots block the blood vessels in the lungs. There are currently three treatment options for patients with CTEPH:
* surgery to remove blood clots from large vessels in the lungs (pulmonary endarterectomy (PEA))
* the use of a small balloon to unblock smaller blood vessels (balloon pulmonary angioplasty (BPA))
* drugs
Patients can also receive a combination of these treatments.
The main question this registry aims to answer are:
* How many patients receive a given kind of treatment?
* How do expert centers combine the different treatments?
* Are patients doing better after they receive a given kind of treatment?
* How many patients are alive 1, 3 and 5 years after they receive a given kind of treatment?
Participants will receive the same treatments that they would receive if they did not participate in the study. During the study, patients will visit their doctors as they would do normally. The doctors will collect information on the patients' health and enter it into the study database. The follow-up time will be at least 3 years for all patients.
Conditions
- Chronic Thromboembolic Pulmonary Hypertension
- CTEPH
Interventions
- PROCEDURE
-
Pulmonary endarterectomy
Surgical removal of a chronic clot from the pulmonary artery
- PROCEDURE
-
Balloon pulmonary angioplasty
Catheter-based intervention to dilate occluded pulmonary vessels through the insertion and inflation of a small balloon
- DRUG
-
Pulmonary hypertension (PH)-specific medication
Treatment with any PH-specific medication, i.e. endothelin receptor antagonists, phosphodiesterase type 5 inhibitors, soluble guanylate cyclase stimulators, drugs acting on the prostanoid pathway and prostaglandin I2 receptor agonists
Sponsors & Collaborators
-
Janssen Pharmaceuticals
collaborator INDUSTRY -
International CTEPH Association
lead OTHER
Principal Investigators
-
Nick H Kim, MD · University of California, San Diego
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-04-12
- Primary Completion
- 2028-04-30
- Completion
- 2028-04-30
Countries
- United States
- Argentina
- Austria
- Belgium
- Brazil
- Canada
- China
- Colombia
- Czechia
- Denmark
- Germany
- India
- Italy
- Japan
- Mexico
- Poland
- Singapore
- Spain
- Turkey (Türkiye)
- United Kingdom
Study Locations
More Related Trials
-
Functional Pulmonary Capillary Surface Area in BPA for CTEPH
NCT05719415 ·Status: RECRUITING ·Phase: NA
-
Registry of Patients With chrOnic thromboemboLic Pulmonary hypErTension
NCT07254078 ·Status: RECRUITING
-
Balloon Pulmonary Angioplasty in Non-operable CTEPH Patients
NCT02964390 ·Status: UNKNOWN ·Phase: NA
-
Hemodynamic Effects of BPA at Rest and During Exercise in CTEPH
NCT04052243 ·Status: UNKNOWN ·Phase: NA
-
Durg Coated Balloon Angioplasty in Infrapopliteal Lesions
NCT05620095 ·Status: RECRUITING
-
Clinical Study of Excimer Laser and Drug Coated Balloon Versus Excimer Laser and Plain Balloon Versus Plain Balloon and Drug Coated Balloon to Treat Femoropopliteal In-stent Restenosis
NCT04365062 ·Status: UNKNOWN ·Phase: NA
-
Endovascular Therapy for Renal Artery Stenosis in China
NCT03080519 ·Status: UNKNOWN ·Phase: NA
-
BPA in CTEPD Without PH
NCT06090838 ·Status: RECRUITING ·Phase: NA
-
Interventional Treatment of Residual Pulmonary Hypertension in Patients After Pulmonary Thromboendarterectomy
NCT02745106 ·Status: UNKNOWN ·Phase: PHASE2
-
International BPA Registry
NCT03245268 ·Status: COMPLETED
-
This Study is a Prospective, Multi-center, Real World, Observational Study, Which Aims at Evaluating Intermediate and Long-term Efficacy of Endovascular Treatment for TASC C&D Aortoiliac Occlusive Disease.
NCT05391815 ·Status: RECRUITING
-
Tack Optimized Drug Coated Balloon Angioplasty Study of the Tack Endovascular System™ in Femoropoliteal Arteries
NCT02802306 ·Status: COMPLETED ·Phase: NA
-
Study to Evaluate the Lower Extremity Intervention With Integrated Embolic Protection Using the Vanguard IEP System
NCT03271710 ·Status: COMPLETED ·Phase: NA
-
Angioplasty of Distal Lesions for Carriers of Inoperable Post-embolic HTP
NCT02844036 ·Status: COMPLETED ·Phase: NA
-
Study of DA+LDD in the Treatment of Femoropopliteal Occlusive Disease
NCT03380650 ·Status: UNKNOWN ·Phase: NA
-
Tack Optimized Balloon Angioplasty Study of the Tack Endovascular System® in Below the Knee Arteries
NCT02942966 ·Status: COMPLETED ·Phase: NA
-
Cutting Balloon Study
NCT01205568 ·Status: COMPLETED ·Phase: NA
-
Development and Application of a New Balloon Catheter for Intraairway Hemostasis
NCT05554731 ·Status: UNKNOWN ·Phase: NA
-
Results of Endovascular Treatment for Infrapopliteal Arterial Occlusive Disease.
NCT06009146 ·Status: UNKNOWN
-
IN.PACT Global Clinical Study
NCT01609296 ·Status: COMPLETED ·Phase: NA
-
Drug-eluting Balloon for Treatment of Non-atherosclerotic Renal Artery Stenosis
NCT04366596 ·Status: UNKNOWN ·Phase: PHASE3
-
Registration Trial of the Drug-coated Balloon for the Symptomatic Cerebral Atherosclerotic Stenosis
NCT06683118 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Shockwave™Peripheral Intravascular Lithotripsy Balloon for Advanced Endovascular Aortic Repair
NCT06332911 ·Status: RECRUITING
-
To Verify the Efficacy and Safety of Rapamycin Coated Peripheral Balloon Catheter in the Treatment of Femoral Popliteal Artery Disease
NCT05662618 ·Status: UNKNOWN ·Phase: NA
-
Outcome and Improvement of Different Treatment in Arteriosclerosis Obliterans
NCT06485622 ·Status: RECRUITING