← Eichor
Study identifier: NCT06500403 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Non-invasive Tools for PSVD Diagnosis

Condition: Non-Cirrhotic Portal Hypertension · Porto-Sinusoidal Vascular Diseases  ·  Sponsor: Nanfang Hospital, Southern Medical University

PhaseN/A
Planned participants1000
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

Patients treated with platinum-based chemotherapy drugs have the probability of developing PSVD. The diagnosis of PSVD depends on liver biopsy. In addition, the level of portal vein pressure has guiding value in the diagnosis and prognosis of PSVD. Many studies have shown that liver and spleen stiffness have high accuracy in diagnosis and prognosis. The purpose of this study is to evaluate the efficacy of the combination of liver and spleen stiffness in the diagnosis of PSVD and to search for effective biomarkers for the diagnosis of PSVD through a single-center, prospective, observational study.

This description comes directly from the study's public registry record.

Talk to the study team

Xiaofeng Zhang  ·  +8618565552050  ·  1282614092@qq.com

Always discuss trial participation with your own doctor first.

Locations (1)

Nanfang hospital, Southern Medical UiversityGuangzhou, Guangdong, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06500403