An Infant Formula Trial on Dietary Management of Infantile Colic
2018年9月7日 更新者:Danone Asia Pacific Holdings Pte, Ltd.
A Randomised, Double Blind, Controlled, Multi-centre Study to Assess the Efficacy of an Infant Formula in the Dietary Management of Infantile Colic
A randomised, double blind, controlled, multi-centre study to assess the efficacy of an infant formula in the dietary management of infantile colic.
研究概览
详细说明
A randomised, double blind, controlled, multi-centre study to assess the efficacy of an infant formula in the dietary management of infantile colic.
The hypothesis of the study is that the test product, compared to the control formula, will reduce the crying time in infants with infantile colic.
The various time points of the outcome are:
V1 (screening : Day -5 to day 0); V2 ( Randomization: Day 0); V3 (Day 7); V4 (Day 21); Phone Call (Day 28); V5 (End -intervention: Day 42); V6 (Day 56)
研究类型
介入性
注册 (实际的)
5
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
3周 至 1个月 (孩子)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- Infants aged 21-56 days (both inclusive);
- Gestation age 37-42 weeks;
- Normal birth weight for gestational age and gender
- 5-minute APGAR score >7;
- Diagnosed with infantile colic ;
- Fully formula fed for at least 7 days before randomisation;
- Written informed consent from the parent and/or legal representative.
Exclusion Criteria:
- Any plausible cause of inconsolable crying as judged by the investigator;
- Presence of non-functional vomiting or failure to thrive;
- Presence of any congenital defects in the gastrointestinal system or other defects preventing oral nutrition;
- Congenital condition and/or previous or current illness/infection and (or) medication use that could interfere with the main study outcomes;
- Known cow's milk protein allergy, lactose intolerance, or galactosaemia; including presence of any allergic manifestations;
- Received any special formula (e.g. lactose-free, hydrolysed protein);
Received any of the following products/medication within 7 days before randomisation:
- Probiotics
- Systemic antibiotics
- Prokinetics
- Proton pump inhibitors
- Twins or triplets or other infant(s) <6 months of age living in the same household;
- Incapability of the parent(s) to comply with the study protocol or investigator's uncertainty about the willingness or ability of the subject to comply with the protocol requirements;
- Current participation in another clinical study involving investigational or marketed products.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:其他
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Intervention group
An infant formula which contains specific hydrolysed proteins with a fat blend, prebiotics mixture, starch and reduced lactose
|
An infant formula which contains specific hydrolysed proteins with a fat blend, prebiotics mixture, starch and reduced lactose
|
|
有源比较器:Control group
Standard cow's milk with prebiotics mixture
|
Standard cow's milk with prebiotics mixture
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Daily inconsolable crying time using data recorded on subject's diaries
大体时间:6 weeks
|
Daily inconsolable crying time over 6 weeks
|
6 weeks
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Daily crying time using data recorded on subject's diaries
大体时间:6 weeks
|
Daily crying time over 6 weeks of intervention
|
6 weeks
|
|
Daily fussing time using data recorded on subject's diaries
大体时间:6 weeks
|
Daily fussing time over 6 weeks of intervention
|
6 weeks
|
|
Daily inconsolable fussing time using data recorded on subject's diaries
大体时间:6 weeks
|
Daily inconsolable fussing time over 6 weeks of intervention
|
6 weeks
|
|
Daily stool frequency using data recorded on subject's diaries
大体时间:6 weeks
|
Daily stool frequency over 6 weeks of intervention
|
6 weeks
|
|
Daily stool consistency using data recorded on subject's diaries
大体时间:6 weeks
|
Daily stool consistency over 6 weeks of intervention
|
6 weeks
|
|
The frequency of subject's GI symptoms of digestion in the 7-day period prior to the visit using the Infant gastrointestinal symptoms questionnaire
大体时间:6 weeks
|
Gastrointestinal symptoms using the Infant gastrointestinal symptoms questionnaire during the 6-week intervention period
|
6 weeks
|
|
The intensity of subject's GI symptoms of digestion in the 7-day period prior to the visit using the Infant gastrointestinal symptoms questionnaire
大体时间:6 weeks
|
Gastrointestinal symptoms using the Infant gastrointestinal symptoms questionnaire during the 6-week intervention period
|
6 weeks
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2017年10月27日
初级完成 (实际的)
2018年7月3日
研究完成 (实际的)
2018年7月3日
研究注册日期
首次提交
2017年10月3日
首先提交符合 QC 标准的
2017年10月31日
首次发布 (实际的)
2017年11月1日
研究记录更新
最后更新发布 (实际的)
2018年9月10日
上次提交的符合 QC 标准的更新
2018年9月7日
最后验证
2018年9月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.