About this trial

The development of Clinical significant PH (CSPH) is a major driver of complications. PPG is the strongest predictor of decompensation . The shortcomings of GPVH measurements and invasiveness has resulted in an area of unmet clinical need. Non-selective beta-blockers (NSBB) have demonstrated efficacy in reducing PH. However, this requires a second invasive procedure, and there is high interindividual variability in the hemodynamic response to NSBB. EUS-guided GPP measurement emerges as a more accurate, accessible and less invasive technique to potentially predict chronic hemodynamic response. The aim of this project is to assess the safety and efficacy of EUS-derived GPP measurement (EUS-GPP) in patients diagnosed with cirrhosis, to assess the acute hemodynamic response through EUS-derived GPP to intravenous propranolol administration in order to determine the patients who would benefit from NSBB treatment in primary prophylaxis to prevent decompensation using a strategy guided by EUS-GPP measurement.

Eligibility criteria

Qualifiers

Patients diagnosed with advanced liver disease with an indication for primary prophylaxis with NSBBs

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

35 Participants
are grouped into 1 trial group

Locations

1
Hospital Universitario Virgen Macarena41009, SevilleSEVILLA, Spain

Sponsors and collaborators

Hospital Universitario Virgen Macarena

Lead sponsor