Verification of Risk Factors of Thrombohemorrhagic Complications in Recipients After Related Liver Transplantation
VORTAL
Verification of Prognostic Risk Factors of Thrombohemorrhagic Complications in Early Follow-up Period in Recipients After Living Related Liver Transplantation
1 other identifier
observational
30
1 country
1
Brief Summary
The aim of the study is to improve the results of related transplantation of the right liver lobe by verifying the general predictors of the development of hemostatic system disorders and optimizing a comprehensive program for thrombohemorrhagic complications preventing.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Apr 2022
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 22, 2022
CompletedFirst Submitted
Initial submission to the registry
December 5, 2023
CompletedFirst Posted
Study publicly available on registry
December 13, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 14, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 16, 2026
December 30, 2025
July 1, 2025
4.6 years
December 5, 2023
December 29, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Thrombosis of vascular anastomosis
Thrombosis of arterial or venous anastomosis after intervention
1 month
Secondary Outcomes (1)
Hemorrhagic complications
1 month
Study Arms (1)
liver transplant group
Interventions
Related transplantation of the right lobe of the liver
Eligibility Criteria
Patients with end stage liver cirrhosis who underwent living related liver transplantation.
You may qualify if:
- Age over 18 years and up to 70 years;
- End stage liver cirrhosis.
You may not qualify if:
- Pregnancy;
- Extrahepatic factors influencing systemic hemostasis;
- Concomitant hematological diseases affecting the hemostatic system;
- Severe concomitant disorders.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Republican specialized scientific and practical medical center of surgery named after academician V.Vakhidov
Tashkent, 100115, Uzbekistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
December 5, 2023
First Posted
December 13, 2023
Study Start
April 22, 2022
Primary Completion (Estimated)
November 14, 2026
Study Completion (Estimated)
December 16, 2026
Last Updated
December 30, 2025
Record last verified: 2025-07