Endoscopic Ultrasound Guided Response Assessment to Non-selective Beta-blockers in the Treatment of Clinically Significant Portal Hypertension

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to learn if endoscopic ultrasound (EUS)-guided portal pressure measurement can determine the treatment response to non-selective beta-blockers (NSBB) in patients with cirrhosis and clinically significant portal hypertension (CSPH). Participants will undergo EUS-guided portal pressure measurement before start of Carvedilol en after three months of treatment. EUS-guided measurements will be paired with transjugular hepatic venous pressure gradient (HVPG) measurement as well as non-invasive tests for assessment of portal hypertension.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Patients with a clinical and/or pathological diagnosis of compensated cirrhosis.

• Patients with suspicion of CSPH and thus indication for NSBB treatment.

• Patients not yet on NSBB therapy.

• Patients willing and able to undergo repeated HVPG and EUS-guided pressure measurements as per protocol.

Locations
Other Locations
Belgium
University Hospital Leuven
RECRUITING
Leuven
Contact Information
Primary
Emma Vanderschueren, MD
emma.vanderschueren@uzleuven.be
0032 16 345918
Backup
Petra Windmolders
petra.windmolders@uzleuven.be
003216 347581
Time Frame
Start Date: 2024-07-17
Estimated Completion Date: 2026-07
Participants
Target number of participants: 24
Treatments
Experimental: EUS-PPG before and after NSBB
Patients will undergo EUS-PPG and HVPG before and after NSBB treatment and will thus serve as their own control.
Related Therapeutic Areas
Sponsors
Leads: Universitaire Ziekenhuizen KU Leuven

This content was sourced from clinicaltrials.gov