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Recruiting Phase 3

Riociguat-Discontinue Effects on Right HEART in CTEPH (RED-HEART)

NCT06922240 · tracked via the Priya Life Science China tracker
Sponsor
Suqiao Yang
Phase
Phase 3
Started
2025-03-21
Last updated
2025-04-30

Condition(s) studied

Chronic Thromboembolic Pulmonary Hypertension

Investigational drug(s) / intervention(s)

Riociguat →Routine Treatment

Riociguat: On the basis of the comprehensive treatment in line with the guidelines, including conventional diuresis, anticoagulation, oxygen inhalation, etc., continue oral administration of riociguat for treatment.

Routine Treatment: On the basis of the comprehensive treatment in line with the guidelines, including conventional diuresis, anticoagulation, oxygen inhalation, etc, and stop taking riociguat

Study summary

Riociguat and balloon pulmonary angioplasty (BPA) are established standard-of-care interventions for inoperable chronic thromboembolic pulmonary hypertension (CTEPH) with comparable evidence levels. However, the optimal combined treatment strategy remains unclear. Specifically, there is no consensus on whether riociguat should be continued long-term after achieving hemodynamic stability with BPA. Additionally, the long-term effects of riociguat discontinuation on right ventricular (RV) structure and function remain poorly characterized, particularly due to the lack of comprehensive noninvasive evaluations integrating cardiac magnetic resonance (CMR) and echocardiography. This prospective study aims to determine the hemodynamic impact of riociguat discontinuation in inoperable CTEPH patients who have achieved BPA treatment endpoints using right heart catheterization (RHC). Evaluate RV remodeling and functional changes after riociguat cessation through multimodal noninvasive imaging (CMR, echocardiography). Assess safety outcomes and identify potential rebound pulmonary hypertension or decompensated RV dysfunction associated with riociguat withdrawal.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥18 years old * CTEPH was diagnosed and one of the following three factors was met: Pulmonary endarterectomy was technically impossible; Pulmonary endarterectomy is technically feasible, but the risk-benefit ratio is poor; Residual/recurrent pulmonary hypertension after pulmonary endarterectomy * Subjects had been treated with BPA and had received a stable dose of riociguat for ≥12 weeks * mPAP \< 30mmHg * Male subjects and female subjects of reproductive age are required to use effective contraception for at least 28 days after signing the informed consent form. Male subjects are not allowed to donate sperm and female subjects are not allowed to breastfeed. * Subjects voluntarily sign written informed consent Exclusion Criteria: * Severe hepatic and renal insufficiency (Child-Pugh Grade C/creatinine clearance \< 30ml/min·1.73m²) * The presence of severe infectious disease or severe bleeding tendency * Combined with pulmonary hypertension of other types than CTEPH * Other pulmonary hypertension targeting drugs are being used * The expected survival time with cancer or other diseases is less than 6 months * Pregnancy, lactation * Subjects are currently participating in an interventional clinical trial * In the investigator's judgment, a subject's medical abnormality, physical condition, or medical history may affect his or her ability to participate in or complete the study

Primary outcome measure(s)

  • Change from Baseline in the Cardiac Output at 6 Months. — Baseline and 6-month follow-up
    Cardiac Output was measured by right heart catheterization.

Trial sites (3)

FacilityCityRegionStatus
Beijing Chao-Yang Hospital Beijing China Recruiting
China-Japan Friendship Hospital Beijing China Recruiting
Beijing Anzhen Hospital Beijing China Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06922240 on ClinicalTrials.gov ↗ ← All trials in China