Determinants of Right Heart Remodeling in Patients With CTEPH or PAH (PRINCEPT)
Primary Purpose
Chronic Thrombo-embolic Pulmonary Hypertension and Pulmonary Arterial Hypertension
Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
magnetic resonance imaging
2D and 3D trans-thoracic echocardiography
Blood samples
Sponsored by
About this trial
This is an interventional other trial for Chronic Thrombo-embolic Pulmonary Hypertension and Pulmonary Arterial Hypertension
Eligibility Criteria
Inclusion Criteria:
- adults (age > 18 years old)
- who give their informed consent for the protocol
- with either CTEPH referred to our insitution for pulmonary arterial endarterectomy. CTEPH is defined by invasive mean pulmonary arterial pressure ≥ 25mmHg at rest, secondary to chronic pulmonary embolism confirmed by computed tomographic (CT) angiography and/or ventilation/perfusion scan, according to the lastest guidelines
- Or with PAH referred to our institution for lung transplant. PAH is defined according to the latest guidelines by an invasive mean pulmonary arterial pressure ≥ 25mmHg, secondary to idiopathic, familial, drug or toxin, or connective tissue disease etiology.
Exclusion Criteria:
- pregnant women
- children
- congenital heart diseases
- contraindications for MRI such as metallic foreign bodies or devices, claustrophobia
- contraindication for surgery
- patients requiring preoperative mechanical assistance such as extracorporeal membrane oxygenation
- patients with pulmonary arterial sarcoma
Sites / Locations
- Hopital Marie LannelongueRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
CTEPH PATIENTS
PAH PATIENTS
Arm Description
Patients undergoing pulmonary endarterectomy for the treatment of chronic thromboembolic pulmonary hypertension (CTEPH).
patients with pulmonary arterial hypertension (PAH) undergoing lung transplantation
Outcomes
Primary Outcome Measures
right ventricular adverse remodeling
postoperative right ventricular adverse remodeling, defined by increase above 10% in end-systolic right ventricular volume indexed on body surface area assessed by cardiac MRI.
Secondary Outcome Measures
Full Information
NCT ID
NCT03205085
First Posted
June 28, 2017
Last Updated
January 21, 2020
Sponsor
Centre Chirurgical Marie Lannelongue
1. Study Identification
Unique Protocol Identification Number
NCT03205085
Brief Title
Determinants of Right Heart Remodeling in Patients With CTEPH or PAH
Acronym
PRINCEPT
Official Title
Determinants of Postoperative Right Heart Remodeling in Patients With Chronic Thrombo-Embolic Pulmonary Hypertension After Endarterectomy, or Pulmonary Arterial Hypertension After Lung Transplantation
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
August 9, 2017 (Actual)
Primary Completion Date
July 1, 2020 (Anticipated)
Study Completion Date
July 1, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Chirurgical Marie Lannelongue
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Right heart failure is the main cause of morbi-mortality in patients with pulmonary hypertension (PH), including patients of chronic thrombo-embolic pulmonary hypertension (CTEPH) or pulmonary arterial hypertension (PAH) etiologies. Endarterectomy is an effective treatment for patients with CTEPH to lower pulmonary pressure. Evidence of postoperative right heart remodeling are contrasted according to the studies and determinants of right heart failure are still unclear. Similarly, few evidence exists on right ventricular remodeling after bilateral lung transplantation for patients with pulmonary arterial hypertension (PAH). Recent evidence have supported the role of inflammation and immunity in the pathophysiology of PAH . While several cytokines have been shown to predict survival , little is known on the implication of inflammation and immunity in postoperative Right Ventricular failure in patients with PAH.
• The specific translational goal of this current project is to elucidate the role of immune biomarkers in 6 months postoperative right heart adverse remodeling in patients with CTEPH or PAH. We speculate that selected immune biomarkers (such as CXCL9, interleukin -18 or interferon) and growth factors (such as HGF) are correlated with mid-term postoperative right heart failure.
All consecutive adults with either CTEPH referred to our center for endarterectomy, or PAH referred for lung transplantation, will be included, aiming for 150 CTEPH and 50 PAH. After inclusion, patients will undergo assessment of right heart dimensions and function by cardiac magnetic resonance imaging (MRI, including 4-Dimensions blood flow sequences) and 2D and 3D trans-thoracic echocardiography (TTE), as well as immune panel analysis. All patients will undergo as part of routine care right heart catheterization within a week after TTE and MRI imaging. On the day of surgery, pulmonary pressure will be measured by right heart catheterization monitoring (as part of routine care) in order to estimate the drop of pressure and to adjust for the extent of endarterectomy for patients with CTEPH. TTE will also be performed on the day of surgery if possible. At 7 days post-endarterectomy or transplant, clinical outcomes will be collected and peripheral blood will be collected. Patients will be prospectively follow-up for 6 months. Death, need for reintervention, duration of vasopressor after surgery and number, duration and cause of readmission will be recorded. At 6 months after surgery, all survivors will undergo the same biological sampling, as well as an 4D MRI and a 2D and 3D TTE. Data of right heart catheterization at 6 months (as part of routine care) will be collected as well.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Thrombo-embolic Pulmonary Hypertension and Pulmonary Arterial Hypertension
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Non-Randomized
Enrollment
150 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
CTEPH PATIENTS
Arm Type
Experimental
Arm Description
Patients undergoing pulmonary endarterectomy for the treatment of chronic thromboembolic pulmonary hypertension (CTEPH).
Arm Title
PAH PATIENTS
Arm Type
Experimental
Arm Description
patients with pulmonary arterial hypertension (PAH) undergoing lung transplantation
Intervention Type
Radiation
Intervention Name(s)
magnetic resonance imaging
Intervention Description
assessment of right heart dimensions and function by cardiac magnetic resonance Imaging.
Intervention Type
Procedure
Intervention Name(s)
2D and 3D trans-thoracic echocardiography
Intervention Description
assessment of right heart dimensions and function by 2D and 3D trans-thoracic echocardiography
Intervention Type
Other
Intervention Name(s)
Blood samples
Intervention Description
Blood samples for assays of immune inflammatory biomarkers (InterLeukin-18, CXCL9 or interferon
Primary Outcome Measure Information:
Title
right ventricular adverse remodeling
Description
postoperative right ventricular adverse remodeling, defined by increase above 10% in end-systolic right ventricular volume indexed on body surface area assessed by cardiac MRI.
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
adults (age > 18 years old)
who give their informed consent for the protocol
with either CTEPH referred to our insitution for pulmonary arterial endarterectomy. CTEPH is defined by invasive mean pulmonary arterial pressure ≥ 25mmHg at rest, secondary to chronic pulmonary embolism confirmed by computed tomographic (CT) angiography and/or ventilation/perfusion scan, according to the lastest guidelines
Or with PAH referred to our institution for lung transplant. PAH is defined according to the latest guidelines by an invasive mean pulmonary arterial pressure ≥ 25mmHg, secondary to idiopathic, familial, drug or toxin, or connective tissue disease etiology.
Exclusion Criteria:
pregnant women
children
congenital heart diseases
contraindications for MRI such as metallic foreign bodies or devices, claustrophobia
contraindication for surgery
patients requiring preoperative mechanical assistance such as extracorporeal membrane oxygenation
patients with pulmonary arterial sarcoma
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
LILIA LAMRANI
Phone
01.40.94.25.54
Ext
33
Email
l.lamrani@ccml.fr
First Name & Middle Initial & Last Name or Official Title & Degree
OLAF MERCIER
Phone
01.40.94.86.95
Email
o.mercier@ccml.fr
Facility Information:
Facility Name
Hopital Marie Lannelongue
City
Le Plessis-Robinson
ZIP/Postal Code
92350
Country
France
Individual Site Status
Recruiting
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
36372884
Citation
Dong ML, Azarine A, Haddad F, Amsallem M, Kim YW, Yang W, Fadel E, Aubrege L, Loecher M, Ennis D, Pavec JL, Vignon-Clementel I, Feinstein JA, Mercier O, Marsden AL. 4D flow cardiovascular magnetic resonance recovery profiles following pulmonary endarterectomy in chronic thromboembolic pulmonary hypertension. J Cardiovasc Magn Reson. 2022 Nov 14;24(1):59. doi: 10.1186/s12968-022-00893-x.
Results Reference
derived
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Determinants of Right Heart Remodeling in Patients With CTEPH or PAH
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