Ignite Creation Date:
2024-10-26 @ 3:35 PM
Last Modification Date:
2024-10-26 @ 3:35 PM
Study NCT ID:
NCT06513780
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-07-08
Brief Title:
A Study of the Correlation Between Portal Vein Thrombosis and Prognosis of Liver Transplantation
Sponsor:
None
Organization:
None
Study Overview
Official Title:
A Study of the Correlation Between Portal Vein Thrombosis and Prognosis of Liver Transplantation
Status:
RECRUITING
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this observational study is to investigate the correlation between portal vein thrombosis PVT and the prognosis of liver transplantation The main questions it aims to address are
What is the prevalence of PVT What are the risk factors associated with PVT What is the prognostic impact of preoperative PVT on liver transplantation
Participants are divided into two groups the PVT group and the non-PVT group The investigators will comparatively analyze the data of both groups estimate the prevalence and risk factors of PVT construct a predictive model for PVT that is applicable in clinical settings and clarify the prognostic effects of PVT
What is the prevalence of PVT What are the risk factors associated with PVT What is the prognostic impact of preoperative PVT on liver transplantation
Participants are divided into two groups the PVT group and the non-PVT group The investigators will comparatively analyze the data of both groups estimate the prevalence and risk factors of PVT construct a predictive model for PVT that is applicable in clinical settings and clarify the prognostic effects of PVT
Detailed Description:
The investigators aim to investigate the prevalence and risk factors of PVT to develop a novel grading or rating system for PVT and to explore the prognostic impact of preoperative PVT in liver transplantation
The investigators will
Recruit patients according to the inclusionexclusion criteria and obtain signed informed consents They will collect demographic and laboratory characteristics and classify patients into the PVT group and the non-PVT group based on preoperative ultrasound andor computed tomography
Collect patients perioperative medical imaging surgical procedures pathology reports postoperative treatments follow-up data and clinical endpoints
Comparatively analyze the data of the PVT and non-PVT groups estimate the prevalence and risk factors of PVT construct a predictive model for PVT that is applicable in clinical settings clarify the prognostic effects of PVT and propose a gradingrating system for PVT
The investigators will
Recruit patients according to the inclusionexclusion criteria and obtain signed informed consents They will collect demographic and laboratory characteristics and classify patients into the PVT group and the non-PVT group based on preoperative ultrasound andor computed tomography
Collect patients perioperative medical imaging surgical procedures pathology reports postoperative treatments follow-up data and clinical endpoints
Comparatively analyze the data of the PVT and non-PVT groups estimate the prevalence and risk factors of PVT construct a predictive model for PVT that is applicable in clinical settings clarify the prognostic effects of PVT and propose a gradingrating system for PVT
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None