跳至主要内容
临床试验/EUCTR2014-004249-29-GB
EUCTR2014-004249-29-GB
进行中(未招募)
1 期

An Open Label, Non-Randomised, Phase II study to Determine if Dabigatran and its Metabolites are Detectable in Breast Milk Following Oral Administration to Non-Breastfeeding Mothers - Dabigatran Presence in Breast Milk (DALMATION)

概览

阶段
1 期
干预措施
未指定
疾病 / 适应症
Future use for VTE prophylaxis.
发起方
The Newcastle Upon Tyne Hospitals NHS Foundation Trust
状态
进行中(未招募)
最后更新
8年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2017年8月21日
结束日期
待定
最后更新
8年前
研究类型
Interventional clinical trial of medicinal product
性别
Female

研究者

入排标准

入选标准

  • Women aged \=18 years
  • Woman has had a vaginal birth (spontaneous or instrumental)
  • Minimum of 48 hours has passed after delivery of the baby/ removal of epidural catheter or spinal anaesthesia
  • Minimum of 24 hours has passed after the decision has been made and documented in the notes to stop breast feeding the baby after starting/trying to start.
  • Hospital inpatient
  • Woman has been offered the opportunity to have a discussion at delivery and in the immediate postnatal period in relation to their feeding choices using the Feeding Your Baby booklet.
  • Decision has been confirmed by the woman to exclusively formula\-feed her baby (including women who have since decided to stop breast\-feeding their baby)
  • Midwife has confirmed the decision with the woman and has documented this in the Feeding Your Baby Booklet held in the medical notes.
  • Normal renal function test – results of the serum creatinine \<90 micro mol/L.
  • Normal liver function tests – results of the serum ALT •Not taking any medication except paracetamol and / or dihydrocodeine. Women who have been given ibuprofen for pain relief after delivery can be included at least 24 hours after the last dose. Women will be advised not to take non\-steroidal anti\-inflammatory drugs (aspirin, ibuprofen, diclofenac, naproxen, indometnacin) for at least 3 days after taking the study treatment)

排除标准

  • Women who are planning to/are breastfeeding
  • Women who are planning to/giving their baby expressed breast milk
  • Women who are unsure of their decision to breast feed or formula feed
  • Women who are unable to provide written informed consent
  • LMWH thromboprophylaxis is indicated
  • Increased risk of bleeding for any reason
  • An increased tendency to bleed (inborn, of unknown cause or due to other medications)
  • Known contra\-indications to dabigatran
  • On\-going treatment with aspirin, NSAIDs or other drugs that affect haemostasis
  • Treatment with oral ketoconazole or itraconazole, medicines to treat fungal infections

结局指标

主要结局

未指定

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