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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06169592
Other study ID # 05122023
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 22, 2022
Est. completion date September 14, 2024

Study information

Verified date April 2024
Source Republican Specialized Scientific and Practical Medical Center of Surgery Named After V. Vakhidov
Contact Azam Babadjanov, Professor
Phone +998901751703
Email azambabadjanov@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date September 14, 2024
Est. primary completion date August 14, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Age over 18 years and up to 70 years; - Signed informed consent for inclusion to the study; - End stage liver cirrhosis. Exclusion Criteria: - Pregnancy; - Extrahepatic factors influencing systemic hemostasis; - Concomitant hematological diseases affecting the hemostatic system; - Severe concomitant disorders.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Liver transplantation
Related transplantation of the right lobe of the liver

Locations

Country Name City State
Uzbekistan Republican specialized scientific and practical medical center of surgery named after academician V.Vakhidov Tashkent

Sponsors (1)

Lead Sponsor Collaborator
Republican Specialized Scientific and Practical Medical Center of Surgery Named After V. Vakhidov

Country where clinical trial is conducted

Uzbekistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Thrombosis of vascular anastomosis Thrombosis of arterial or venous anastomosis after intervention 1 month
Secondary Hemorrhagic complications Any hemorrhagic complications after intervention 1 month
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