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Investigating the effect of using the blood of a brain dead liver donor patient during liver transplantation on the liver recipient patient

Investigating the effect of using the blood of a brain dead liver donor patient during liver transplantation on a liver recipient patient at Abu Ali Sina organ transplant center in 2023

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211008052699N2
Enrollment
124
Registered
2023-07-23
Start date
2023-06-22
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

LIVER TRANSPLANT. Surgical operation with transplant of whole organ as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure

Interventions

Intervention 1: Intervention group: blood transfusion from a brain dead donor to a patient undergoing liver transplantation.The outcome of patients after transplantation is checked and recorded based

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Stability in vital signs (heart rate less than 100 R/M, systolic pressure more than 100 mmHg). Hemoglobin level above 11 Age 18 to 40 years having blood group and RH between the donor and the recipient The same immunological conditions between donor and recipient in terms of cytomegaloviruses Matching based on sender and receiver cross match Transplantation from a brain dead donor Whole liver transplant Stability of vital signs at the time of liver transplant surgery Failure to receive inotrope before the transplant procedure No grade 3 or 4 encephalopathy before transplantation Age between 18 and 40 years Absence of evidence of portal vein thrombosis in preoperative examinations Liver transplant for the first time Not having a history of hepatic vein thrombosis (Bodekiari syndrome) or other diseases with high blood coagulation potential.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bleeding rate during liver transplant surgery and after surgery (first 24 hours). Timepoint: During the operation and up to 24 hours after the operation. Method of measurement: Questionnaire.;The amount of blood injected during the liver transplant operation and after the operation (first 24 hours). Timepoint: During the operation and up to 24 hours after the operation. Method of measurement: Questionnaire.;The rate of hepatic artery thrombosis during liver transplantation and after the operation (the first two weeks after transplantation). Timepoint: During the transplant operation up to two weeks after the transplant. Method of measurement: Doppler ultrasound, CT abdominal angiography.;Mortality rate during liver transplant surgery and after surgery (first 30 days after transplant). Timepoint: The first 30 days after liver transplantation. Method of measurement: questionnaire.;The degree of initial dysfunction of the transplanted liver (during the first week). Number of days of hospitalization in ICU after transplantation. Timepoint: The first week after transplantation. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactalireza shamsaefar

Shiraz University of Medical Sciences

eslamian67@yahoo.com+98 71 3448 0000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026