CTRI/2024/02/063141招募中4 期
Comparative Evaluation of Three Vitamin D3 Formulations for Sequential Improvement of Vitamin D3 Levels throughout a period of 3-Months. - NI
Dr Roshan Pawar0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 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
- •1.Willing to provide voluntary written informed consent.
- •2.If an individual is unable to provide informed consent due to reasons such as illiteracy, a Legal Authorized Representative (LAR) will be required to provide written informed consent.
- •3.Male or Female subjects between 18 to 65 years of age (both inclusive)
- •4.Vitamin D3 deficiency less than 20 ng/ml
- •5.Willing and able to comply with the protocol.
排除标准
- •1.Any Surgery or hospitalization within 28 days before enrolment
- •2.Known hypersensitivity to any component of the investigational product and other medications used in this study
- •3.Patients already on supplementation of calcium and/or Vitamin D
- •4.Patients suffering from acute or chronic infection(s)
- •5.BMI greater than 40 Kg/m2
- •6.Female patients who are pregnant or nursing
- •7.Patients with H/O concurrent disease or conditions like ESRD, pre-existing liver cell failure, terminally ill cancer or critically ill patients, which in the opinion of the investigator does not allow participation of the patient in this study
- •8.Has participated in any other clinical trial and received experimental medications within 4 weeks prior to screening
研究者
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