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临床试验/ISRCTN95769543
ISRCTN95769543已完成未知

Studying Accompaniment model Feasibility and Effectiveness: a prospective, non-inferiority study of the effectiveness of self-managed medication abortion

Ibis Reproductive Health0 个研究点目标入组 1,352 人开始时间: 2019年8月15日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
1,352

研究概览

简要总结

2020 Other publications in https://pubmed.ncbi.nlm.nih.gov/33109230/ feasibility results from pilot study (added 29/10/2020) 2020 Protocol article in https://pubmed.ncbi.nlm.nih.gov/33444174/ main study protocol (added 18/01/2021) 2021 Results article in https://pubmed.ncbi.nlm.nih.gov/34801131/ (added 22/11/2021) 2023 Results article in https://pubmed.ncbi.nlm.nih.gov/37411022/ (added 07/07/2023)

研究设计

研究类型
Observational

入排标准

性别
Female

入选标准

  • 1. Contacted the accompaniment group seeking information about induced abortion for their own pregnancy
  • 2. At least 13 years of age
  • 3. Able to give informed consent
  • 4. Able to speak the local language
  • 5. Meets accompaniment group eligibility criteria for starting medication abortion process (i.e. no known contraindications to medication abortion)
  • 6. Starting a new medication abortion process

排除标准

  • 1. Are experiencing ongoing symptoms (bleeding, cramping) from a previous abortion attempt prior to study enrollment
  • 2. Have a known ectopic pregnancy or symptoms of an ectopic pregnancy
  • 3. Do not want to share their contact information with study staff
  • 4. Do not want to be contacted again by the hotline or by study staff
  • 5. Are not willing to comply with study procedures
  • 6. Cannot access a phone and private location to answer questions during follow-up

研究者

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