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临床试验/CTRI/2024/04/066269
CTRI/2024/04/066269尚未招募4 期

Assessment of Safety and Efficacy of Romiplostim in Live Donor Liver Transplant Recipients- A Prospective Randomized Open Label Trial

Amrita School of Pharmacy1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2024年5月10日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
24
试验地点
1
主要终点
To determine the number of days required for normalization of the platelet count in the romiplostim group compared to the control group following live donor liver transplantation

研究概览

简要总结

Following liver transplantation, thrombocytopenia is the common accompaniment within 0-5 days. Recovery to normalcy may take over 2-3 weeks in 60% of patients. Thrombocytopenia during this period may lead to bleeding from the operated or remote sites such as the brain. • Additionally, it is thought that thrombocytopenia has a propensity to exaggerate infection leading to graft failure, even to mortality. This is because platelets contain several growth factors, platelet-derived growth factors, insulin-like growth factors, hepatocyte growth factors, vascular endothelial growth factors as well as numerous cytokines.  Romiplostim is more or less proven in thrombocytopenia following stem cell transplantation However it’s role in liver transplantation is not known . Our study aims to assess the efficacy and safety of romiplostim in live donor liver transplantation

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Patient with the age group of 18-65years.
  • Patients with a platelet count below 40000 Patient who signed the informed consent form.

排除标准

  • Pregnancy, age under 18 or over 65, ongoing multiple organ failure, antiplatelet therapy, suspected/ diagnosed heparin-induced thrombocytopenia or innate/acquired thrombophilia.
  • Patients with myelodysplastic or myeloproliferative syndrome, hematological malignancy, and aplasia diagnosed on bone marrow.
  • severe liver cirrhosis with a Child-Pugh score superior to 6, or a medical history of pulmonary embolism/stroke in the previous 6 months were also excluded.

结局指标

主要结局

To determine the number of days required for normalization of the platelet count in the romiplostim group compared to the control group following live donor liver transplantation

时间窗: Baseline line(before drug administration) | Post drug administration day 1 to day 14

次要结局

  • To compare the incidence of thrombosis in the portal vein, hepatic vein & and hepatic artery in both groups.(To quantify and analyse the platelet-derived growth factor, hepatocyte growth factor and vascular endothelial growth factor in romiplostim and control group.)

研究者

发起方
Amrita School of Pharmacy
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr S Sudhindran

Amrita institute of Medical Sciences Kochi

研究点 (1)

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