RV Conductance Catheter Assessment During Balloon Pulmonary Angioplasty
NCT04444973 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 20
Last updated 2023-11-22
Summary
Balloon pulmonary angioplasty (BPA) treats patients with inoperable chronic thromboembolic pulmonary hypertension (CTEPH). Intra-procedural markers of success to guide the intervention are lacking. The investigators propose to measure right ventricular (RV) pressure volume loops invasively and measure biomarkers at intervals during the course of a course of BPA. These data will be analysed to define load independent indices of RV functional improvement, cross correlated with biomarker data and be used to calibrate non-invasive assessment of ventriculo-arterial coupling by cardiac magnetic resonance imaging (CMR) to better detect responders of BPA and pulmonary endarterectomy (PEA).
Conditions
- Chronic Thromboembolic Pulmonary Hypertension
Interventions
- PROCEDURE
-
Balloon pulmonary angioplasty
Balloon dilatation of sub segmental pulmonary artery web disease
Sponsors & Collaborators
-
Papworth Hospital NHS Foundation Trust
lead OTHER_GOV
Principal Investigators
-
Stephen P Hoole, MD · Royal Papworth Hospital
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-01-01
- Primary Completion
- 2024-12-31
- Completion
- 2024-12-31
Countries
- United Kingdom
Study Locations
More Related Trials
-
Use and Safety of the LUTONIX® Drug Coated Balloon Catheter in Arteries of the Lower Extremity
NCT02043951 ·Status: TERMINATED
-
Hemodynamic Effects of BPA at Rest and During Exercise in CTEPH
NCT04052243 ·Status: UNKNOWN ·Phase: NA
-
Initial Dual Oral Combination Therapy Versus Standard-of-care Initial Oral Monotherapy Prior to Balloon Pulmonary Angioplasty in Patients With Inoperable Chronic Thromboembolic Pulmonary Hypertension
NCT04780932 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Clinical Study of Balloon Pulmonary Angioplasty for Patients With Chronic Thromboembolic Pulmonary Hypertension
NCT04326777 ·Status: UNKNOWN ·Phase: NA
-
BPA in CTEPD Without PH
NCT06090838 ·Status: RECRUITING ·Phase: NA
-
Endothelial Function in Lower Extremity Bypass Grafts
NCT00759707 ·Status: COMPLETED ·Phase: NA
-
Functional Pulmonary Capillary Surface Area in BPA for CTEPH
NCT05719415 ·Status: RECRUITING ·Phase: NA
-
A Single Arm Trial Evaluating the BARD Lutonix Drug-Coated Balloon (LTX DCB) for Treatment of Femoropopliteal Arteries
NCT02720003 ·Status: COMPLETED ·Phase: NA
-
Interventional Treatment of Residual Pulmonary Hypertension in Patients After Pulmonary Thromboendarterectomy
NCT02745106 ·Status: UNKNOWN ·Phase: PHASE2
-
LEVANT 2 Safety Registry
NCT01790243 ·Status: COMPLETED ·Phase: NA
-
LEVANT I, The Lutonix Paclitaxel-Coated Balloon for the Prevention of Femoropopliteal Restenosis
NCT00930813 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Safety and Effectiveness of the Device "Nit-Occlud® PDA-R"
NCT01063712 ·Status: COMPLETED ·Phase: PHASE2
-
Budd-Chiari Syndrome in China: Balloon Angioplasty Alone or Combined With Stent Placement?
NCT02201485 ·Status: COMPLETED ·Phase: NA
-
POWER: Pulse Intravascular Lithotripsy (Pulse IVL) to Open Vessels With Calcific Walls and Enhance Vascular Compliance and Remodeling
NCT05192473 ·Status: UNKNOWN ·Phase: NA
-
Investigating the Safety and Clinical Performance of Seven iVascular Devices for Endovascular Intervention in the Popliteal and/or Infrapopliteal Arteries
NCT05267548 ·Status: UNKNOWN
-
BPA vs. PEA in CTEPH
NCT05110066 ·Status: RECRUITING ·Phase: NA
-
Angioplasty + SBCV vs. Angioplasty Alone for Femoropopliteal Artery Stenosis
NCT02568293 ·Status: UNKNOWN ·Phase: NA
-
Non-invasive Peri- and Postoperative Monitoring of Femoral Artery Balloon Angioplasty
NCT02725307 ·Status: COMPLETED
-
Drug-eluting Balloon for Treatment of Non-atherosclerotic Renal Artery Stenosis
NCT04366596 ·Status: UNKNOWN ·Phase: PHASE3
-
Study Comparing Lutonix AV Drug Coated Balloon vs Standard Balloon for Treatment of Dysfunctional AV Fistulae
NCT02440022 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Effectiveness Study With a New PDA Occluder for Closure of Patent Ductus Arteriosus
NCT01479218 ·Status: COMPLETED ·Phase: NA
-
Real-World Registry Assessing the Clinical Use of the Lutonix 035 Drug Coated Balloon Catheter
NCT02424383 ·Status: COMPLETED ·Phase: NA
-
Treatment of Patients With Takayasu Arteritis Complicated With Pulmonary Artery Involvement
NCT05388682 ·Status: RECRUITING
-
Post Approval Study Investigating Lutonix Drug Coated Balloon for Treatment of Dysfunctional Arteriovenous Fistulae
NCT03506308 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Cutting Balloon Study
NCT01205568 ·Status: COMPLETED ·Phase: NA