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NCT02356250

A Pilot Study: Defining Peripheral Endothelial Function in Portal Hypertensive Cirrhotic Patients

Withdrawn Last updated 26 July 2018
What this trial tests

trial in Portal Hypertension. Withdrawn.

Timeline
18 February 2015
Primary endpoint
29 November 2016
29 November 2016

Quick facts

Lead sponsorEyal Ashkenazi
StatusWithdrawn
Study typeOBSERVATIONAL
Start date18 February 2015
Primary completion29 November 2016
Estimated completion29 November 2016

Conditions studied

Sponsor

Eyal Ashkenazi

Who can join

Adults 18 to 75, any sex, with Portal Hypertension or Cirrhosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Rationale for the study: To try and define PEF in cirrhotic patients with CSPH, and maybe to try to find a correlation between HVPG ( hepatic vein pressure gradient ) result and PEF result in a way that the result of the PEF test will be able to predict if a patient has CSPH (yes of no). By this, to try and develop a portable office-based device that can produce immediate results in a non-invasive manner in cirrhotic patients and help in evaluating prognosis in these patients in a noninvasive manner. Aim: The aim of this study is to try and characterize the peripheral endothelial function (PEF) in patient with cirrhosis and CSPH. This will be evaluated by measuring the PEF in every patient before evaluating his HVPG level in a hemodynamic study.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Portal Hypertension

Currently open trials in the same condition.

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Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing