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临床试验/NCT02016495
NCT02016495已完成4 期

Efficacy of Magnesium and Alpha Lipoic Acid Supplementation in Reducing Premature Uterine Contractions

AGUNCO Obstetrics and Gynecology Centre1 个研究点 分布在 1 个国家开始时间: 2013年12月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
试验地点
1
主要终点
Number of women with frequent and persistent episodes of preterm uterine contractions associated with pain

研究概览

简要总结

To evaluate whether a combined supplementation of magnesium and lipoic acid is able to significantly reduce the incidence of uterine contractions and related episodes of hospitalization in pregnant women.

详细描述

Primary prevention of preterm labor is based on the early identification of risk factors and on appropriate treatments. Although several drugs are currently used, the identification of effective and safe agents able to improve both maternal and fetal health is still warranted.

In this study the efficacy a formulation based on magnesium and alpha-lipoic acid has been compared with placebo to evaluate the incidence of reduction of preterm delivery.

Three hundred pregnant women at 14-34 weeks of gestation were enrolled and randomly divided to receive a daily single tablet containing magnesium and alpha-lipoic acid supplement or placebo until delivery.

研究设计

研究类型
Interventional

入排标准

年龄范围
23 Years 至 41 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 14-34 weeks of gestation

排除标准

  • Preexisting diabetes mellitus
  • Systolic blood pressure >140mm Hg
  • hepatitis
  • Diagnosed alcohol or chemical dependency

研究组 & 干预措施

Magnesium + Lipoic Acid

Active Comparator

干预措施: Magnesium plus alpha-lipoic acid (Dietary Supplement)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Number of women with frequent and persistent episodes of preterm uterine contractions associated with pain

时间窗: From baseline (beginning of the treatment) until delivery

Number of women with sporadic episodes of preterm uterine contraction

时间窗: From baseline (beginning of the treatment) until delivery

Number of women needed for hospital admission for threatened preterm labour

时间窗: From baseline (beginning of the treatment) until delivery

次要结局

未报告次要终点

研究者

发起方
AGUNCO Obstetrics and Gynecology Centre
申办方类型
Other
责任方
Sponsor

研究点 (1)

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