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Assessment of Right Ventricular-Pulmonary Arterial Coupling in Schistosomiasis-Associated Pulmonary Arterial Hypertension

Assessment of Right Ventricular-Pulmonary Arterial Coupling in Schistosomiasis-Associated Pulmonary Arterial Hypertension

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07707193
Acronym
Sch-PAH RV-PA
Enrollment
50
Registered
2026-07-16
Start date
2026-07-01
Completion date
2027-07-01
Last updated
2026-07-16

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

Conditions

Schistosomiasis

Brief summary

Pulmonary Arterial Hypertension is a progressive and potentially fatal cardiopulmonary disorder characterized by remodeling of the pulmonary vasculature, progressive elevation of pulmonary vascular resistance (PVR), and eventual right ventricular (RV) failure. According to the 2022 European Society of Cardiology/European Respiratory Society (ESC/ERS) guidelines, pulmonary hypertension is currently defined hemodynamically by a mean pulmonary arterial pressure (mPAP) \>20 mmHg measured by right heart catheterization, while pulmonary arterial hypertension is additionally characterized by pulmonary arterial wedge pressure (PAWP) ≤15 mmHg and PVR \>2 Wood units. Schistosomiasis-associated pulmonary arterial hypertension (Sch-PAH) is classified within Group 1 PAH and represents one of the most important causes of PAH in endemic regions, particularly in developing countries such as Egypt and Brazil. Schistosomiasis is considered the second most prevalent parasitic disease worldwide after malaria, affecting more than 200 million individuals globally. Chronic hepatosplenic schistosomiasis may lead to porto-systemic shunting, allowing parasite eggs to embolize into the pulmonary circulation, triggering chronic inflammation, endothelial dysfunction, and pulmonary vascular remodeling. The pathological changes observed in Sch-PAH resemble those seen in idiopathic PAH, including medial hypertrophy, intimal fibrosis, and plexiform lesions. However, several studies suggest that patients with Sch-PAH may exhibit better long-term survival compared with idiopathic PAH despite comparable pulmonary hemodynamic impairment. The mechanisms underlying this relatively favorable prognosis remain incompletely understood. Right ventricular adaptation to increased afterload is currently recognized as one of the principal determinants of prognosis in PAH.

Interventions

PROCEDUREright heart catheterization for measure pulmonary artery pressure

right heart catheterization for measure pulmonary artery pressure Through swan ganz catheter

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients above 18 year diagnosed with schistozomiasis through history of exposure , serology , positive stool antigens ,Symmers' periportal fibrosis (the "clay pipe-stem" appearance) or Splenomegaly and suspected pulmonary hypertension through Probability Score" approach based on the 2022 ESC/ERS

Exclusion criteria

* All patients below 18 years old. * Left ventricular systolic or diastolic dysfunction. * Significant left-sided valvular heart disease. * severe chronic lung disease such as, Chronic obstructive pulmonary disease (COPD) ---- GOLD 4 and severe Interstitial lung disease (ILD). * Chronic Thromboembolic Pulmonary Hypertension. * Congenital heart diseases. * Severe hepatic or renal impairment unrelated to schistosomiasis. * Hemodynamically unstable patients. * Poor echocardiographic window preventing adequate RV assessment. * Active infection or acute systemic illness. * Refusal to participate in the study. * Significant arrhythmias affecting hemodynamic assessment (e.g., uncontrolled atrial fibrillation). * Previous heart or lung transplantation. * Pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Right ventricular-pulmonary arterial coupling quantified by the TAPSE/PASP ratio measured by transthoracic echocardiography at baseline1 yearThe tricuspid annular plane systolic excursion to pulmonary artery systolic pressure (TAPSE/PASP) ratio will be measured by standard transthoracic echocardiography in all participants at the study assessment. TAPSE will be measured in millimeters (mm) using M-mode echocardiography, and PASP will be estimated in mmHg from the peak tricuspid regurgitation velocity. The TAPSE/PASP ratio (mm/mmHg) will be calculated for each participant and reported as a continuous variable (mean ± standard deviation or median \[interquartile range\], depending on data distribution).

Countries

Egypt

Contacts

CONTACTAhmed M Sayed, Assistant lecturer
ahmed_mahmoud4@med.sohag.edu.eg+201095630589

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 17, 2026