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The Effect of Monitoring PVP on Clinical Outcomes in Patients With PH

The Effect of Monitoring Portal Venous Pressure on Clinical Outcomes in Patients With Portal Hypertension: a Prospective, Single-center, Observational Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04820166
Enrollment
200
Registered
2021-03-29
Start date
2021-03-12
Completion date
2025-12-31
Last updated
2021-03-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Portal Hypertension

Brief summary

The complications associated with portal hypertension in cirrhosis are the main cause of death in patients with cirrhosis. The level of portal venous pressure is closely related to the prognosis of patients. HVPG (hepatic venous pressure gradient) is the gold standard for predicting portal venous pressure and an important indicator for evaluating the efficacy of NSBBS. However, monitoring HVPG has many limitations,and the clinical application is also limited to a certain extent. Therefore, this study intends to clarify the guiding value of monitoring portal venous pressure in the clinical diagnosis and treatment of portal hypertension patients through a single-center, prospective and observational study. Therefore, this study intends to clarify the guiding value of monitoring portal venous pressure in the clinical diagnosis and treatment of portal hypertension patients through a single-center, prospective and observational study. At the same time, to explore the correlation between HVPG and PPG in cirrhosis patients at different stages and different etiologies, and to evaluate the role of spleen stiffness in predicting the severity of esophageal and gastric varices in patients with portal hypertension, and to find biomarkers to predict the risk of complications related to portal hypertension.

Interventions

OTHERmonitoring portal pressure gradient or hepatic venous pressure gradient

measuring portal pressure gradient or hepatic venous pressure gradient regularly

Sponsors

Nanfang Hospital, Southern Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years

Inclusion criteria

* With chronic liver disease * Age 18-80 years * Patients who require a portal pressure measurement at the discretion of the treating physician * Voluntarily signed informed consent

Exclusion criteria

* With serious cardiopulmonary disease or other diseases affect survival * With severe renal dysfunction * Concomitant portal vein cavernous degeneration or extensive portal vein thrombosis * Women who are planning to become pregnant or who are pregnant or breastfeeding * The researcher judged that it was not suitable to participate in this study

Design outcomes

Primary

MeasureTime frameDescription
Gastroesophageal varices bleedingthree yearsPatients with gastroesophageal varices has hematemesis or melena, and active bleeding or red sign can be seen under endoscopy
Ascitesthree yearsPeritoneal effusion was seen under ultrasound
Hepatic encephalopathythree yearsPatients with altered consciousness or unresponsiveness, accompanied by elevated blood ammonia

Secondary

MeasureTime frame
Death or final follow-up time (3 years)three years

Countries

China

Contacts

Primary ContactXiaofeng Zhang
1282614092@qq.com+8618565552050

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026