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Image-based Multi-scale Modeling Framework of the Cardiopulmonary System: Longitudinal Calibration and Assessment of Therapies in Pediatric Pulmonary Hypertension

Image-based Multi-scale Modeling Framework of the Cardiopulmonary System: Longitudinal Calibration and Assessment of Therapies in Pediatric Pulmonary Hypertension

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03564522
Enrollment
35
Registered
2018-06-21
Start date
2017-04-01
Completion date
2023-07-28
Last updated
2024-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congenital Heart Disease, Pediatric Congenital Heart Disease, Pulmonary Hypertension

Brief summary

This study looks to develop a multi-scale computational model of Pulmonary Hypertension, this clinical model will be calibrated using longitudinal, retrospectively and prospectively acquired human clinical data.

Detailed description

Pulmonary hypertension (PH) is a complex disorder associated with elevated pulmonary arterial pressure. Unlike systemic hypertension, PH is difficult to detect in routine physical examinations and the current gold standard for diagnosing PH is through invasive right heart catheterization. Prolonged PH results in functional, structural and anatomical changes in the right ventricle (RV), large pulmonary arteries, and the pulmonary micro-circulation that ultimately lead to decompensated RV failure and death. Unlike in systemic hypertension, for which patients have effective pharmacological management of blood pressure for decades, PH prognosis remains poor with 15% mortality within 1 year on modern therapy. Our current understanding of PH has largely been obtained through animal models and clinical studies. However, surgical banding or chronic hypoxia animal models do not fully reproduce the etiology of human PH, whereas invasive clinical measurements of pulmonary vascular resistance (PVR), stiffness and ventricular elastance provide limited insight into disease progression. Therefore, there is a pressing need to develop a multi-scale (MS) computational model that can couple the short term (e.g. hemodynamics) and long-term G&R interactions between the RV and the pulmonary circulation. The overall goals of this project are to use the framework to (1) describe the time course of the biomechanical alterations and (2) identify the key mechanical culprits associated with PH-induced heart failure so that clinical interventions can be targeted against them.

Interventions

PROCEDUREcardiac catheterization

cardiac catheterizations will be clinically indicated and the study will collect this clinical data.

RADIATIONCardiac MRI

If clinically indicated, the study will collect data from MRIs.

Sponsors

Michigan State University
CollaboratorOTHER
Nationwide Children's Hospital
CollaboratorOTHER
National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
University of Michigan
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
6 Years to 25 Years

Inclusion criteria

* Patients has been clinically diagnosed with pulmonary hypertension (\>25 mmHg) or patient is a biopsy-proven non-rejecting cardiac transplant recipient * Receiving partial or full care from pediatric cardiology team at Mott Children's Hospital (may have a primary cardiologist elsewhere).

Exclusion criteria

* Girls and women who are pregnant or actively trying to become pregnant * Patients with significant neurocognitive impairment that precludes their ability to sign a consent form * Patient has a contraindication to right-heart catheterization (RHC) examination, which includes patients with hypoxia and those who have difficulty maintaining supine position for the procedure. * Patients with the following genetic syndromes:Trisomy 21 if unable to assent or consent, Trisomy 18,Trisomy 13, Other genetic syndromes at the discretion of the Primary Investigator * Patients with unrepaired single ventricles (i.e., Pre-Fontan physiology) * Patients who have heart failure and are deemed to be high risk to undergo tests that require sedation/anesthesia. * Patients who require IV sedation or general anesthesia for research only MRI * Patients with a pacemaker/internal defibrillator will be excluded from MRI PORTION ONLY

Design outcomes

Primary

MeasureTime frameDescription
3D volumetric data (mL/m2)1 hourModeling framework will be validated using 3D volumetric data (mL/m2) gathered via cardiac MRI
Cardiopulmonary Flow (mL/beat)1 hourModeling framework will be validated using cardiopulmonary flow (mL/beat) gathered via cardiac MRI
Mean Pressure (mmHg)2 hoursModeling framework will be validated using pressures (mmHg) gathered via cardiac catheterization

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026