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临床试验/ISRCTN70616901
ISRCTN70616901已完成未知

A randomised controlled trial to determine the effectiveness of bridging from emergency to regular contraception: the Bridge–it study

niversity of Edinburgh0 个研究点目标入组 636 人开始时间: 2017年3月20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
636

研究概览

简要总结

2019 Protocol article in https://pubmed.ncbi.nlm.nih.gov/31672711/ protocol (added 22/10/2020) 2020 Results article in https://pubmed.ncbi.nlm.nih.gov/33189179/ results (added 16/11/2020) 2021 Results article in https://pubmed.ncbi.nlm.nih.gov/33949940/ (added 06/05/2021) 2022 Results article in https://pubmed.ncbi.nlm.nih.gov/35149574/ process evaluation (added 16/05/2023)

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • Current inclusion criteria as of 31/01/2019:
  • 1. Intake of oral emergency contraception (1.5 mg or 3 mg Levonorgestrel)
  • 2. Capacity to give informed consent to participate in the trial which includes adherence to trial requirements
  • 3. Willing to give contact details and be contacted at 4 months by phone or text or e-mail or post
  • 4. Willing to give identifying data sufficient to allow data linkage with NHS registries
  • 5. Female aged 16 years or over
  • Previous inclusion criteria:
  • 1. Intake of oral emergency contraception (1.5 mg Levonorgestrel)
  • 2. Willing to participate in the trial
  • 3. Willing to give contact details and be contacted at 4 and 12 months by phone or text or e-mail or post
  • 4. Willing to give identifying data sufficient to allow data linkage with NHS registries
  • 5. Female 16 years or older

排除标准

  • Current exclusion criteria as of 31/01/2019:
  • 1 Contraindications to the POP (there are very few)
  • 2 On medication that interacts adversely with POP
  • 3. Already using a hormonal method of contraception
  • 4. Require interpreting services
  • 5. If pharmacist has concerns about non-consensual sex
  • Previous exclusion criteria:
  • 1. Not willing to provide contact details or personal data sufficient to allow identification/linkage with NHS registries
  • 2. Contraindications to the POP (there are very few)
  • 3. On medication that interacts adversely with POP
  • 4. Age under 16
  • 5. Already using a hormonal method of contraception
  • 6. Require interpreting services

研究者

发起方
niversity of Edinburgh

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