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NCT07563608Recruiting

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

Source: ClinicalTrials.gov · Last updated 4 May 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
70 (estimated)
First submitted
22 Apr 2026
Start date
Nov 2018
Primary completion date
Sept 2026
Lead sponsor
Fondazione IRCCS Policlinico San Matteo di Pavia
NCT number
NCT07563608

What you commit to

  • Study type: Observational
  • Planned participants: 70
  • From Nov 2018 to the primary completion date, Sept 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Presence of valvular or congenital heart disease
  • Acute infections within the month preceding the cardiological evaluation

Other

  • WHO functional class IV

Who the study is looking for

  • 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

Age in the registry: 18 years to 75 years · Sex: All

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fondazione IRCCS Policlinico San Matteo di Pavia
Coordinator of this site? Confirm its status
PaviaItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.