Effects of DHEA in Pulmonary Hypertension

Last updated: November 19, 2024
Sponsor: Rhode Island Hospital
Overall Status: Active - Not Recruiting

Phase

2

Condition

Pulmonary Arterial Hypertension

Williams Syndrome

Stress

Treatment

DHEA tablet

Placebo

Clinical Study ID

NCT03648385
R01HL141268
  • Ages > 18
  • All Genders

Study Summary

The goal of this crossover trial is to determine whether the study drug dehydroepiandrosterone (DHEA) improves right ventricular longitudinal strain measured by cardiac magnetic resonance imaging at 18 weeks compared to placebo and to assess side effects and safety in pulmonary arterial hypertension.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Diagnosis of PAH that is 1) idiopathic, 2) heritable or 3) associated with connective tissue disease, congenital systemic-to-pulmonary shunt, porto-pulmonary hypertension, drug or toxin use.

Documentation of the following at any time prior to study entry:

  • mPAP ≥ 25 mmHg at rest, pulmonary capillary wedge pressure or left ventricularend-diastolic pressure ≤ 15 mmHg, and PVR > 3 Wood units

  • Pulmonary function testing documenting forced expiratory volume in one second/forcedvital capacity ratio ≥ 70% predicted and total lung capacity ≥ 70% predicted

  • If TLC is mildly reduced (60%<TLC%<70%), computerized tomography (HRCT or non-HRCT)documenting no significant interstitial lung disease may be used to fulfill thisrequirement.

  • Chest tomography documenting no more than moderate parenchymal lung disease withclinician designated WHO I PAH and meeting both TLC and FEV1/FVC criteria.

  • Normal or low probability V/Q scan

  • If no V/Q scan is available, a CT angiogram documenting the absence ofthromboembolic disease may be used, provided the subject meets diagnostic PAHcriteria

Exclusion

Exclusion Criteria:

  • Age < 18 years old

  • PAH associated with human immunodeficiency virus infection

  • New background PAH therapy within 12 weeks

  • Significant dose change in background PAH therapy within 12 weeks.

  • Untreated severe obstructive sleep apnea diagnosed by polysomnography

  • Evidence of left-sided valvular disease or systolic dysfunction on echocardiogram (≥moderate mitral or aortic disease or LV ejection fraction ≤ 50%)

  • Glomerular filtration rate <40 mls/min/1.73m2

  • Child-Pugh Class C cirrhosis

  • Untreated hypo- or hyper-thyroidism

  • Pregnant or breastfeeding

  • Active or planned use of hormone supplements, oral contraceptive pills, hormonaltherapies

  • History of breast, ovarian, uterine, testicular or prostate cancer

  • Current use of another investigational PAH therapy

  • Contraindication to MRI (e.g., metal device or fragment)

  • History of significant non-adherence or circumstance which would threaten ability tocomply with cross-over design and study visit schedule

Study Design

Total Participants: 24
Treatment Group(s): 2
Primary Treatment: DHEA tablet
Phase: 2
Study Start date:
January 09, 2019
Estimated Completion Date:
December 31, 2025

Study Description

Pulmonary hypertension (PH) is a heterogenous clinical disease characterized foremost by an abnormal increase in pulmonary artery pressure. Pulmonary vasculopathy, characterized by pathologic remodeling and vasoconstriction of the pulmonary arterioles, results in progressive dyspnea, exercise intolerance, right ventricular (RV) failure, and death. Female sex is the strongest clinical risk factor for PAH, with a 4:1 female-to-male ratio reported from the largest registry. Despite the increased risk of PAH in women, women with PAH have better survival than men. RV function is an important cause of morbidity and mortality in PAH as well as highly prevalent heart and lung diseases, but determinants of the RV response are entirely unknown. We and others have shown that female sex is associated with better RV systolic function in both health and disease, including PAH and left heart failure. Targeted PAH therapy leads to greater improvements in RVEF (demonstrated after just several months of treatment) in women as compared to men and partially explains better outcomes in women. Demonstration that DHEA has direct RV and sex-based effects will support the hypothesis that sex hormones play an important role in disease pathogenesis and provide insight into sex hormone manipulation as a treatment strategy in PAH.

The goal of this crossover trial is to correlate sex and sex hormones (particularly DHEA) to pulmonary vascular and RV phenotype differences in men and women with PAH. The study seeks to leverage a safe and available hormone treatment to gain further insight into 1) RV effects (a novel and critical end point in PH and PAH), 2) effects on two key PAH pathways in vivo and in vitro as a means for understanding sex-based differences in PAH, and 3) efficiency planning for a future Phase II parallel trial of DHEA as a novel treatment strategy in PAH.

Connect with a study center

  • Rhode Island Hospital Pulmonary Hypertension Center

    Providence, Rhode Island 02903
    United States

    Site Not Available

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