CTRI/2019/11/021993招募中1 期
Randomized control trial to assess the efficacy and safety of NRL/2019/5PNK withmicronutrient fortification to promote growth, health and wellbeing in children. - NI
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试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Children Aged 06 - 11 years inclusive (both gender)
- •Consent: Understanding of the study and willingness to participate as evidenced by subjectâ??s
- •parents and/or legal guardianâ??s voluntary written informed consent.
- •Compliance: Understands and is willing, able and likely to comply with all study procedures
- •and restrictions.
排除标准
- •Subject has a known allergy or intolerance to the study product or ingredients or is on a
- •special diet and cannot consume the study product
- •Subject has a current illness requiring hospitalization
- •Subject has a gastrointestinal infection and/or acute diarrhea at the time of inclusion in the
- •Subject is currently taking medication that could affect absorption/metabolism of study
- •product or weight of the child. Exception: Topical/ocular steroids will be permitted during the
- •Subject is diagnosed with recurrent respiratory infections due to cystic fibrosis,
- •immunodeficiency syndromes, and congenital abnormalities of the respiratory tract, congenital
- •lung and ciliary abnormalities, an unsuspected foreign body and asthma. (As per history and
- •documentation in the medical records)
- •Subject has active tuberculosis, acute hepatitis B or C or HIV, malignancy (as per history and documentation in the medical records) as per discretion of investigation
- •Subject has a history of diabetes mellitus (as per history and documentation in the medical
- •Subject has been on antibiotic therapy within the last one month before start of the study
- •(before study Day 1)
- •Subject has dysphagia, aspiration risk, and difficulty in swallowing due to acquired /
- •congenital abnormalities that would hamper oral intake of the study product. (As per history and
- •documentation in the medical records)
- •Subject has a clinically significant nutritional deficiency requiring specific treatment with any
- •other nutritional supplement (not study product) as diagnosed by the investigator.
研究者
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