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Uptake and Acceptability of Home-use of Mifepristone for Medical Abortion

G

Gynuity Health Projects

Status

Completed

Conditions

Termination of Pregnancy

Treatments

Drug: Mifepristone

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The primary aim of this study is to assess the acceptability of home-use mifepristone for termination of pregnancy among women who choose it and their providers. The investigators' secondary aims are to assess rates of follow-up, adherence, efficacy, complications, lost productivity, and to estimate the minimum proportion of women who choose home-use over clinic use of mifepristone.

Enrollment

615 patients

Sex

Female

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Reproductive age women seeking abortion services.
  • Eligible women will be in general good health and assessed by a clinician to have an intrauterine pregnancy less than 64 days L.M.P on the day mifepristone will be taken.
  • Participants must be eligible for medical abortion according to clinician and clinic standards.
  • In the United States, women only 18 years and older will be eligible to participate, unless the study site obtains a waiver to include minors.

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

615 participants in 2 patient groups

clinic administration of mifepristone
No Intervention group
home administration of mifepristone
Experimental group
Treatment:
Drug: Mifepristone

Trial contacts and locations

7

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Data sourced from clinicaltrials.gov

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