Prevalence, Pathogenesis, and Prognosis of Pulmonary Hypertension in Dialysis Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorFondazione IRCCS Policlinico San Matteo di Pavia

About this trial

This prospective multicenter longitudinal study aims to investigate the prevalence, pathogenesis, and prognosis of pulmonary hypertension in patients with end-stage renal disease undergoing chronic hemodialysis. The research seeks to identify specific clinical factors and biomarkers like angiopoietin-2 that contribute to the development of this condition, while evaluating the prognostic value of right ventricular function measured via TAPSE. Participants undergo a standardized screening echocardiogram the day after their intermediate dialysis session to determine the probability of pulmonary hypertension. Those identified as high-risk receive further diagnostic confirmation through right heart catheterization, respiratory function tests, and lung scans to clarify the underlying etiology. The protocol also evaluates the hemodynamic impact of high-flow arteriovenous fistulas and volume overload on pulmonary pressures. Clinical follow-up is conducted at baseline and subsequently at 6, 12, and 24 months to monitor patient outcomes and standardize therapeutic management according to established European guidelines.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

WHO functional class IV

Presence of valvular or congenital heart disease

Acute infections within the month preceding the cardiological evaluation

Trial population

The study population consists of adult patients (18-75 years old) with end-stage renal disease who have been receiving stable extracorporeal hemodialysis for at least six months at participating multicenter dialysis units.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Prevalence of pulmonary hypertension and its subtypes in patients undergoing chronic hemodialysis

Time frame
Baseline (enrollment)

Secondary outcomes

Other outcomes

Sponsors and contacts

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