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临床试验/NCT06789640
NCT06789640尚未招募不适用

Impact of Vitamin C Supplementation on the Hospital Outcomes in Children Undergoing Corrective Heart Surgery for Congenital Heart Diseases

Cairo University0 个研究点目标入组 20 人开始时间: 2025年2月19日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
20
主要终点
The improvemnents of Ejection Fraction between the two groups

研究概览

简要总结

Vitamin C will be given before admission in the immediate preoperative preceding 7 days (the dose 30 -45 mg per day ) in oral drops preparations

Inflammatory markers including CRP , TLC ,PNI , GPS NLR will be checked on admission and on discharge and compared between cases and controls Hospital length stay will also be compared between the two groups

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
— 至 7 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Children in the first two years who will be for corrective surgery for heart diseases congenital heart diseases
  • •Pediatric patients whose parents or caregivers agree to be enrolled in the study.
  • •Risk Adjustment for Congenital Heart Surgery -1 (RACHS-1) for Evaluation of Mortality in Children Undergoing Cardiac Surgery : the first two categories (Thiagarajan and C. Laussen 2015)

排除标准

  • •Pediatric patients with associated comorbid conditions.

研究组 & 干预措施

The control group

Placebo Comparator

A placebo will be given before admission in the immediate preoperative preceding 7 days (the dose 30 -45 mg per day ) in oral drops preparations

Inflammatory markers including CRP , TLC ,PNI , GPS NLR will be checked on admission and on discharge and compared between cases and controls Hospital length stay will also be compared between the two groups

干预措施: Placebo (Other)

Interventional

Experimental

Vitamin C will be given before admission in the immediate preoperative preceding 7 days (the dose 30 -45 mg per day ) in oral drops preparations

Inflammatory markers including CRP , TLC ,PNI , GPS NLR will be checked on admission and on discharge and compared between cases and controls Hospital length stay will also be compared between the two groups

干预措施: Vitamin C (Other)

结局指标

主要结局

The improvemnents of Ejection Fraction between the two groups

时间窗: 7-10 days

Each group wil be evaluated for the eiection fraction before and after the operation and the improvement will be compared

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Hoda Atef Abdelsattar Ibrahim

Hoda Atef Abdelsattar Ibrahim

Cairo University

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