CALIPSO: Cardiac Assessment by PV Loop in IPAH and Scleroderma PAH

Sponsor
Johns Hopkins University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04610788
Collaborator
National Heart, Lung, and Blood Institute (NHLBI) (NIH)
100
1
56.5
1.8

Study Details

Study Description

Brief Summary

This observational study is being done to understand why people with scleroderma can develop pulmonary arterial hypertension (high blood pressure in the lungs, abbreviated PAH) and a weak heart muscle (heart failure). The study will also help the investigators understand why people with PAH from an unknown cause (called idiopathic PAH, or IPAH) can also develop a weakened heart muscle. The response of the right side of the heart or right ventricle (RV) to standard PAH therapy in scleroderma-associated PAH and in IPAH will be assessed. Blood and tissue samples will be collected from research participants during participants' normal standard of care procedures. People with scleroderma-associated PAH or idiopathic cause (IPAH) who need a right heart catheterization may join this study.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Patients with scleroderma associated pulmonary hypertension (with or without interstitial lung disease) have a worse prognosis compared to patients with idiopathic pulmonary arterial hypertension (IPAH). The investigators have discovered through a previous protocol that patients with scleroderma associated pulmonary hypertension (SSc-PAH) have intrinsic right ventricular (RV) contractile dysfunction compared with patients with idiopathic pulmonary hypertension (IPAH) despite similar afterload imposed by the pulmonary vasculature. Patients with scleroderma or presumed/known IPAH who are clinically referred for right heart catheterization (RHC) will undergo, in addition to a clinically indicated RHC, state-of-the-art Pressure-Volume (P/V) Loop Assessment and RV biopsy for research purposes. The investigators will also do a standard pathologic assessment of the RV tissue (H&E, special staining, electron microscopy), microvascular density measurements using immunohistochemistry techniques and isolated skinned myocyte experiments. Additional experiments will include proteomics, genomics/genetics, and RV protein and microRNA expression. The investigators will compare these findings in both groups (IPAH and SSc-PAH), before and after standard treatment for 6 months, in order to fully understand the differences in how the RV adapts to pressure overload and reasons for impaired RV function in SSc-PAH as well as identifying potential therapeutic targets.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    100 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Understanding Right Ventricular Heart Failure in Scleroderma and Idiopathic Pulmonary Arterial Hypertension
    Actual Study Start Date :
    Apr 15, 2019
    Anticipated Primary Completion Date :
    Dec 31, 2023
    Anticipated Study Completion Date :
    Dec 31, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    SSc-PAH Group

    Scleroderma patients referred for a clinically indicated right heart catheterization (RHC).

    IPAH Group

    Presumed/known IPAH patients referred for a clinically indicated right heart catheterization (RHC).

    Outcome Measures

    Primary Outcome Measures

    1. Right Ventricular Function as assessed by RHC [Baseline]

      Assessed on the clinical RHC as normal, moderately reduced, or severely reduced.

    2. Change in pulmonary vascular resistance [Baseline and 6months]

      Assessed as improved or decreased after 6 months by comparing the change in pulmonary vascular resistance in Wood units on the clinical RHC.

    3. Change in arterial elastance [Baseline and 6 months]

      Assessed as improved or decreased after 6 months by comparing the change in arterial elastance in pressure volume (PV) loops.

    4. Change in myofilament contractility [up to 4 years]

      Assessed as Normal or Abnormal after studying the collected samples in lab. Abnormal can be either reduced or increased; i.e. hyper- or hypo-contractile.

    5. Change in calcium sensitivity [up to 4 years]

      Assessed as either increased- or decreased- sensitivity after 6 months, by studying the collected samples in lab.

    Secondary Outcome Measures

    1. Number of genes expressed [up to 4 years]

      Gene expression as assessed by observing presence of microRNA in the lab.

    2. Number of proteins expressed [up to 4 years]

      Protein expression as assessed by observing post-translational modification of candidate proteins in the lab.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 100 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients 18 years or older with clinically diagnosed scleroderma or presumed/known idiopathic pulmonary hypertension.
    Exclusion Criteria:
    • Patients found to have secondary pulmonary hypertension (PH due to left heart failure) on clinical RHC.

    • Hemodynamically unstable patients (systolic blood pressure < 90mmHg, vasopressor requirement).

    • Patients whom are unable to give consent for themselves.

    • Patients with RV clot or septal aneurysm will be excluded.

    • In order to undergo the clinical right heart catheterization procedures, pregnancy testing (urine or serum) is standard of care.

    • Pregnancy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Johns Hopkins Baltimore Maryland United States 21287

    Sponsors and Collaborators

    • Johns Hopkins University
    • National Heart, Lung, and Blood Institute (NHLBI)

    Investigators

    • Principal Investigator: Paul Hassoun, MD, Johns Hopkins University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Johns Hopkins University
    ClinicalTrials.gov Identifier:
    NCT04610788
    Other Study ID Numbers:
    • NA_00049022
    • R01HL114910-06
    First Posted:
    Nov 2, 2020
    Last Update Posted:
    Oct 28, 2021
    Last Verified:
    Oct 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 28, 2021