跳至主要内容
临床试验/CTRI/2025/03/082642
CTRI/2025/03/082642招募中不适用

PERIOPERATIVE ANALGESIC STRATEGIES IN PAEDIATRIC LIVER TRANSPLANT RECIPIENTS

Dr. Rela institute and medical centre1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2026年3月9日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
50
试验地点
1
主要终点
To determine the requirement of perioperative opioids in paediatric liver transplant recipients

研究概览

简要总结

Pain score will be assessed using the following age appropriate scales

Assessment will be done by independent assessors using dedicated scores.

Peak pain score, total dosage of dexmedetomidine and opioids, average duration of analgesic requirement and details of rescue drugs with dosages used will be recorded during the study period.

Complications such as hemodynamic changes requiring dose modifications or discontinuation of drugs, gastrointestinal symptoms such as nausea, vomiting, constipation, ileus will be recorded.

Vomiting will be recorded at 24, 48, 72 hours as per vomiting score (0: no nausea, no vomiting; 1: nausea alone; 2: one episode of emesis; and 3: two or more episodes of emesis)

研究设计

研究类型
Observational

入排标准

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

入选标准

  • All paediatric liver transplant recipients undergoing liver transplantation.

排除标准

  • Patients not willing for participation Multiorgan transplantation Re-exploration on Postoperative day 3 and beyond Re-intubation on postoperative day 3 and beyond.

结局指标

主要结局

To determine the requirement of perioperative opioids in paediatric liver transplant recipients

时间窗: Postoperative Day 0 to day 3 after liver transplant surgery

次要结局

  • To determine the need for the first rescue analgesic in the postoperative period(In the first 3 days following liver transplantation)

研究者

发起方
Dr. Rela institute and medical centre
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Susan Paulin

Dr Rela Institute And Medical Centre

研究点 (1)

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