Chart Review Study of Medical Abortion

NCT02841072 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 579

Last updated 2016-07-21

No results posted yet for this study

Summary

The primary objective of this study is to document the rates of success and serious complications among women having outpatient medical abortions with 200 mg mifepristone + 800 buccal misoprostol at 64-70 days of gestation.

Conditions

  • Abortion, Medical

Sponsors & Collaborators

  • Gynuity Health Projects

    lead OTHER

Principal Investigators

  • Elizabeth Raymond, MD, MPH · Gynuity Health Projects

Eligibility

Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2016-04-30
Completion
2016-04-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02841072 on ClinicalTrials.gov