CTRI/2010/091/001359招募中1 期
A non-comparative, single center study to characterise in-vivo slow release of DTPA tablet in humans
Defence R&D Organisation0 个研究点目标入组 8 人开始时间: 待定最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
- 入组人数
- 8
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. Adults (18-70 years of age)
- •2. On no medication
- •3. Normal swallowing reflux
- •4. Ability to swallow whole tablets
- •5. Ability to remain empty stomach for at least 8 hours
排除标准
- •1. Patients with gastric conditions: medical or surgical
- •2. Patients with gall bladder disease or surgery
- •3. Those unable to lie down in stable condition for scintigraphy
- •4. Pregnant & lactating women or women of child bearing potential not using medically accepted methods of contraception.
- •5. Patients with clinically significant renal, respiratory, cardiac, gastrointestinal, hepatic, endocrine or hematological disorders.
- •6. Patients with abnormalities in gastric function or emptying
- •7. Patients who have any medical condition which in the judgement of the investigator may render them in appropriate for participation in the trial.
- •8. Patients who have received any other investigational drug for the last 3 months
研究者
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