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临床试验/ACTRN12618001472268
ACTRN12618001472268已完成未知

Diagnostic accuracy of PremaQuick in detection of preterm labor in symptomatic women.

Ahmadi Hospital, Kuwait Oil Company (KOC), Kuwait.0 个研究点目标入组 244 人开始时间: 2018年9月3日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
244

研究概览

简要总结

Results: The PremaQuick test had 95.1% sensitivity, 97.5% specificity, 97.5% positive predictive value, 95.2% negative predictive value, and 96.3% accuracy in detection of preterm labor. The PremaQuick had significantly higher true negative rate, specificity, positive predictive value, and overall accuracy in detection of preterm labor compared to cervical length< 25 mm. Conclusion: The PremaQuick is an accurate bedside test in detection of preterm labor in women presented with threatened preterm labor. It had 95.1% sensitivity, 97.5% specificity, 97.5% positive predictive value, 95.2% negative predictive value, and 96.3% overall accuracy in detection of preterm labor. The PremaQuick had significantly higher true negative rate, specificity, positive predictive value, and overall accuracy in detection of preterm labor compared to cervical length< 25 mm.

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Diagnosis

入排标准

年龄范围
20 Years 至 40 Years(—)
性别
Female

入选标准

  • Inclusion criteria includes; Pregnant women with singleton pregnancy, intact membranes, between 24-36 weeks+6, presented with regular uterine contractions lasting at least 30 seconds and occurring at least four times per 30 minutes with significant cervical changes on digital examination (cervical dilatation less than 3 cm, cervical effacement less than or equal 50%).

排除标准

  • Exclusion criteria includes; pregnant women equal or more than 37 weeks, twins or triplets, dilated cervix equal or more than 3 cm, rupture of fetal membranes, congenital fetal anomalies or intra uterine fetal demise or ante-partum hemorrhage.

研究者

发起方
Ahmadi Hospital, Kuwait Oil Company (KOC), Kuwait.

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