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临床试验/NCT06484634
NCT06484634已完成不适用

Role of Low-Molecular-Weight Heparin in Unexplained Recurrent Pregnancy Loss

RESnTEC, Institute of Research1 个研究点 分布在 1 个国家目标入组 175 人开始时间: 2023年12月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
175
试验地点
1
主要终点
Efficacy of Low-Molecular-Weight Heparin

研究概览

简要总结

Using low-molecular-weight heparin (LMWH), outcomes such as live birth rate and the occurrence of pregnancy complications are some of the variables reported in some studies, with varying degrees of success. The present study aimed to compare the role of LMWH in unexplained recurrent pregnancy loss.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 44 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Pregnant females between 18 and 44 years of age
  • Gestational age above 8 weeks
  • A history of ≥3 consecutive first trimester pregnancy losses

排除标准

  • Patients with systemic lupus erythematosus
  • Positive IgG and IgM anticardiolipin antibodies
  • Positive for thrombophilia screening
  • Any platelet function abnormality or a previous thromboembolic event requiring anticoagulant therapy (including heparin, aspirin or warfarin)
  • Sensitive to acetylsalicylic acid, heparin, or warfarin
  • Patients with any genetic, anatomical, or hormonal cause of recurrent pregnancy loss

研究组 & 干预措施

LMWH Group

Experimental

Women received a daily dose of 40 mg of Low Molecular Weight Heparin subcutaneously.

干预措施: Low molecular weight heparin (Drug)

结局指标

主要结局

Efficacy of Low-Molecular-Weight Heparin

时间窗: 32 weeks

Efficacy was labeled as yes in terms of live births after the age of viability, i.e., 24 weeks of gestation.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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