JPRN-jRCTs042180102已完成2 期
Preterm Labor Prevention, Multicenter study for Maternal Cervical Pessary - LOVE MOM trial
Ozaki Yasuhiko0 个研究点目标入组 237 人开始时间: 2018年3月18日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 237
研究概览
简要总结
The results of this trial suggested that cervical pessary did not reduce preterm delivery, but may delay shortening of cervical length. Vaginal discharge was increased by using cervical pessary, no other adverse events were observed. There were no cases of intrauterine fetal demise in both groups. Cervical pessary may shorten duration of hospitalization and medication. In conclusion, cervical pessary may become one of a choice of prophylactic treatment for preterm delivery.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 20age old 至 ot applicable（—）
- 性别
- Female
入选标准
- •1)Pregnant women after 20 weeks gestation, who is disgnosed threatened miscarriage or threatened premature labor.
- •2)Cervical length of 25mm or less.
- •3)Women with informed consent for participation in this trial.
排除标准
- •1)Women with multiple pregnant.
- •2)Majior fetal anomalies.
- •3)Painful regular uterine contractions.
- •4)Active vaginal bleeding.
- •5)Placenta previa.
- •6)Cervical myoma.
- •7)History of cone biopsy or cervical cerclage in situ.
- •8)Other pregnant women when study doctores conclude that they are not eligible for study enrollment.
研究者
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