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临床试验/NCT01257672
NCT01257672已完成3 期

Oral Ondansetron vs Domperidone for Symptomatic Treatment of Vomiting During Acute Gastroenteritis in Children: Multicentre Randomized Controlled Trial

IRCCS Burlo Garofolo15 个研究点 分布在 1 个国家目标入组 356 人开始时间: 2011年7月最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
356
试验地点
15
主要终点
Percentage of patients needing nasogastric or intravenous rehydration after symptomatic oral treatment failure, defined as vomiting or fluid refusal after the second attempt of ORT.

研究概览

简要总结

Vomiting in children with acute gastroenteritis is a major factor of failure of oral rehydration therapy. Effective symptomatic treatment of vomiting would lead to an important reduction in the use of Intravenous Fluid Therapy. Available evidence on symptomatic treatment of vomiting shows the efficacy of the most recently registered molecule (ondansetron) but a proper evaluation of antiemetics drugs largely used in clinical practice, such as domperidone, is lacking.

The aim of this multicentre, double-blind randomized controlled trial is to compare the efficacy of ondansetron and domperidone for the symptomatic treatment of vomiting in children with acute gastroenteritis who have failed Oral Rehydration Therapy.

详细描述

Vomiting in children with acute gastroenteritis (AG) is not only a direct cause of fluid loss but it is also a major factor of failure of oral rehydration therapy (ORT). Physicians who provide care to paediatric patients in the emergency department (ED) usually prescribe intravenous fluid therapy (IVT) for mild or moderate dehydration when vomiting is the major symptom. Thus, effective symptomatic treatment of vomiting would lead to an important reduction in the use of IVT and, consequently, of the duration of hospital stay and of frequency of hospital admission. Available evidence on symptomatic treatment of vomiting shows the efficacy of the most recently registered molecule (ondansetron) but a proper evaluation of antiemetics drugs largely used in clinical practice, such as domperidone, is lacking.

The aim of this multicentre, double-blind randomized controlled trial conducted in paediatric Emergency Departments is to compare the efficacy of ondansetron and domperidone for the symptomatic treatment of vomiting in children with AG who have failed Oral Rehydration Therapy.

The trial results would provide evidence on the efficacy of domperidone, which is largely used in clinical practice despite the lack of proper evaluation and a controversial safety profile, as compared to ondansetron, which is not yet authorized in Italy despite evidence supporting its efficacy in treating vomiting. The trial results would contribute to a reduction in the use of IVT and, consequently, in hospital admissions in children with AG. The design of this RCT, which closely reflect current clinical practice in EDs, will allow immediate transferability of results

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
1 Year 至 6 Years(Child)
性别
All
接受健康志愿者

入选标准

  • age from 1 to 6 years;
  • presumptive clinical diagnosis of acute gastroenteritis in patients with vomiting, with or without diarrhoea;
  • more than three episodes of non-bilious, non-bloody vomiting within the previous 24 hours;

排除标准

  • treatment with antiemetics or antidiarrhoic drugs in the 6 hours prior to access to ED;
  • underlying chronic diseases (eg, malignancy, gastroesophageal reflux, migraine, renal failure, hypoalbuminemia, liver disease);
  • severe dehydration: weight loss>10% or standardized clinical dehydration score >=18 for children aged 12-24 months and >=16 for older children;
  • known hypersensitivity to ondansetron or domperidone;
  • previous enrolment in the study.

研究组 & 干预措施

placebo

Placebo Comparator

placebo, syrup, one dose

干预措施: placebo (Drug)

ondansetron

Experimental

ondansetron, syrup, 0,15 mg/Kg of body weight, 1 dose

干预措施: Ondansetron (Drug)

domperidon

Active Comparator

domperidone, syrup, 0,5 mg/Kg of body weight, one dose

干预措施: Domperidone (Drug)

结局指标

主要结局

Percentage of patients needing nasogastric or intravenous rehydration after symptomatic oral treatment failure, defined as vomiting or fluid refusal after the second attempt of ORT.

时间窗: 6 hours

次要结局

  • Percentage of subjects needing hospital admission for the same illness;(48 hours)
  • Percentage of subjects needing observation stay for more than 6 hours for the same illness(48 hours)
  • Total emesis duration in the 3 allocation groups;(48 hours)
  • Number of episodes of vomiting in the 3 treatment groups during the follow-up period(48 hours)
  • Percentage of subjects presenting adverse events(48 hours)

研究者

发起方
IRCCS Burlo Garofolo
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ronfani Luca

MD

IRCCS Burlo Garofolo

研究点 (15)

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