Pulmonary hypertension in adults on chronic hemodialysis: prevalence, causes, and prognosis
Official title: Prevalence, Pathogenesis, and Prognosis of Pulmonary Hypertension in Dialysis Patients
Run by Fondazione IRCCS Policlinico San Matteo di Pavia · NCT07563608 · Data updated 2026-11-12
This study will test how common pulmonary hypertension is and what causes it in adults on long-term hemodialysis, using heart imaging, catheter measurements, and blood markers to see who is at higher risk.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 75 Years |
| Sex | All |
| Enrollment | 70 (estimated) |
| Sponsor | Fondazione IRCCS Policlinico San Matteo di Pavia Academic / other |
| Locations | 1 site (Pavia, Lombardy) |
| Status | Recruiting |
| Started | November 10, 2018 |
| Main results expected | September 2026 |
| Study ends | September 2026 |
| Registry record updated | May 4, 2026 |
| Trial ID | NCT07563608 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18–75 who have been on stable extracorporeal hemodialysis for at least 6 months, dialyzed two or three times per week, and able to provide written informed consent are ideal candidates.
✕Probably not a fit
Patients with WHO functional class IV, significant valvular or congenital heart disease, recent acute infection, those on other dialysis modalities, or those unable to attend the single center visits are unlikely to benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a prospective multicenter longitudinal observational study of adults with end-stage renal disease receiving chronic extracorporeal hemodialysis. Participants receive a standardized screening echocardiogram the day after an intermediate dialysis session to estimate pulmonary hypertension probability, and those at high risk undergo confirmatory right heart catheterization, lung imaging, and respiratory function testing. The protocol measures biomarkers such as angiopoietin-2 and quantifies right ventricular function (TAPSE) to explore pathogenesis and prognostic value. The study also examines the hemodynamic effects of high-flow arteriovenous fistulas and volume overload with clinical follow-up at baseline, 6 months, and 12 months.
Why it matters
Potential benefit: If successful, the findings could help identify dialysis patients at highest risk for pulmonary hypertension and support earlier, targeted monitoring or interventions to improve outcomes.
How similar studies have gone: Previous observational work has linked dialysis-related factors, arteriovenous fistulas, and volume overload to pulmonary hypertension, but prospective multicenter data linking biomarkers like angiopoietin-2 and TAPSE to prognosis remain limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients aged between 18 and 75 years * Patients on stable extracorporeal hemodialysis for at least 6 months * Dialysis frequency of two or three times per week * Ability to provide written informed consent Exclusion Criteria: * WHO functional class IV * Presence of valvular or congenital heart disease * Acute infections within the month preceding the cardiological evaluation
Where it's running
-
Fondazione IRCCS Policlinico San Matteo di Pavia
Pavia, Lombardy, Italy Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.