跳至主要内容
临床试验/CTRI/2024/12/078312
CTRI/2024/12/078312已完成不适用

FAST TRACKING IN PEDIATRIC LIVING DONOR LIVER TRANSPLANT-A road less travelled…..

Dr Amit Singhal1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2024年12月31日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
28
试验地点
1
主要终点
Our primary outcome is to evaluate the early extubation rate after liver transplant in the paediatric population and demonstrate its safety across all ages.

研究概览

简要总结

We will perform a retrospective observational study and analyse the data of paediatric patients (Aged 3 months -10 years) who underwent LDLT from January 2022 to June 24. Our primary outcome is to evaluate the early extubation rate after liver transplant in the paediatric population and demonstrate its safety across all ages. Our secondary outcome is to determine predictive factors for successful early extubation in this population. Graphpad PRISM version will be used to analyse the data

Paediatric patients who underwent LDLT will be enrolled in the study. They will be divided into two groups - The early extubation (EE) group (extubated on-table or ≤4 hours postoperatively) and the delayed extubation (DE) group (mechanically ventilated > 4 hours postoperatively). Patients will be compared based upon demographic characteristics, intraoperative and postoperative data.

We hypothesise that fast-tracking in paediatric patients is feasible and safe.

研究设计

研究类型
Observational

入排标准

年龄范围
3.00 Month(s) 至 10.00 Year(s)(—)
性别
All

入选标准

  • Paediatric patients (Aged 3 months to 10 years) who underwent living donor liver transplants from January 2022 to June 2024.

排除标准

  • Patients with acute liver failure and hepatic encephalopathy grade 2 or above will be excluded from the analysis.

结局指标

主要结局

Our primary outcome is to evaluate the early extubation rate after liver transplant in the paediatric population and demonstrate its safety across all ages.

时间窗: 30 days

次要结局

  • Our secondary outcome is to determine predictive factors for successful early extubation in this population.(30 days)

研究者

发起方
Dr Amit Singhal
申办方类型
Other [Non funded study]
责任方
Principal Investigator
主要研究者

Dr Amit Singhal

BLK Max Superspeciality Hospital

研究点 (1)

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