ISRCTN41598423已完成未知
QUIDS – Quantitative Fibronectin to help Decision-making in women with Symptoms of Preterm Labour
niversity of Edinburgh and NHS Lothian ACCORD0 个研究点目标入组 2,924 人开始时间: 2015年10月27日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 2,924
研究概览
简要总结
2018 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/29674373 protocol 2019 Results article in https://www.ncbi.nlm.nih.gov/pubmed/31395241 Qualitative results (added 12/08/2019) 2021 Other publications in https://pubmed.ncbi.nlm.nih.gov/34228732/ Development and validation of a risk prediction model (added 30/07/2021) 2021 Funder report results in https://pubmed.ncbi.nlm.nih.gov/34498576/ (added 10/09/2021)
研究设计
- 研究类型
- Observational
入排标准
- 性别
- Female
入选标准
- •1. Women with signs and symptoms of preterm labour 24-34 weeks (or earlier gestation if the fetus is considered potentially viable) in whom hospital admission, inter-hospital transfer or treatment (antenatal steroids, tocolysis or magnesium sulphate) is being considered
- •2. Signs and symptoms may include any or all of the following:
- •2.1. Back pain
- •2.2. Abdominal cramping
- •2.3. Abdominal pain
- •2.4. Light vaginal bleeding
- •2.5. Vaginal pressure
- •2.6. Uterine tightenings or contractions
- •2.7. Cervical effacement or dilatation
排除标准
- •1. Women who have moderate or severe vaginal bleeding
- •2. Women who have cervical dilatation greater or equal to 3cm
- •3. Women with confirmed rupture of membranes
- •4. Sexual intercourse, vaginal examination or transvaginal ultrasound in the preceding 24 hours factors can invalidate results and so these women will be initially excluded from the study. They can later be included if still symptomatic after 24 hours, when fFN accuracy will be restored
研究者
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