ACTRN12623001123639尚未招募Unknown
Determining the optimal dose of omega-3 fatty acids in pregnancy for women with moderate status
适应症
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 入组人数
- 300
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 16 Years 至 o limit（—）
- 性别
- Female
入选标准
- •Singleton pregnancy < 21 weeks gestation
- •Able to give informed consent
- •Randomised Controlled Trial (RCT) Groups only:
- •Identified as having an omega-3 fatty acid status in the lower end of the moderate range (defined as 3.7% to 4.0%% total fatty acids in serum)
- •Reference groups only:
- •Women with low omega-3 status (serum omega-3 <3.7% total fatty acids and supplemented with 800mg DHA + 100mg EPA per day)
- •OR Women with sufficient or replete status (serum omega-3 >4.3% total fatty acids) and taking no more than 250 mg per day of omega-3 from supplements.
排除标准
- •Allergy to fish
- •Enrolled in another fatty acid intervention trial throughout pregnancy.
- •Currently taking heparin (Clexane)
研究者
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