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Clinical Trials/ISRCTN97410750
ISRCTN97410750
Completed
未知

A randomised controlled trial on Efficacy of mifepristone followed by 6-8 hours versus 24 hours vaginal misoprostol in Early Medical Abortions (< 63 days gestation)

Calthorpe Clinic (UK)0 sites1,200 target enrollmentMarch 6, 2009

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Calthorpe Clinic (UK)
Enrollment
1200
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 6, 2009
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Calthorpe Clinic (UK)

Eligibility Criteria

Inclusion Criteria

  • 1\. Ability to give informed written consent
  • 2\. Women who are 18 years and older
  • 3\. Requesting abortion and eligible for legal termination of pregnancy
  • 4\. Duration of pregnancy not more than 63 days (counted from the first day of the last menstrual period) in a normal 28\-day cycle or verified by ultrasound
  • 5\. The pregnancy is single and intrauterine (single sac)
  • 6\. Agree to be able to be contacted by telephone (i.e. mobile telephone)
  • 7\. Women with limited understanding of English will be included only in the quantitative study where interpreters are available

Exclusion Criteria

  • 1\. Any indication of serious past or present ill health will be considered a contraindication for recruitment to the study
  • 2\. Suspicion of any pathology of pregnancy (e.g. molar, non\-viable pregnancy, threatened abortion)
  • 3\. Current participation in a drug\-related trial
  • 4\. Non\-English\-speaking women for the qualitative study
  • 5\. Women under the age of 18 years

Outcomes

Primary Outcomes

Not specified

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