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Study of Clinic-based vs. Self-use of a Misoprostol-only Regimen for Induced Abortion

NCT04242212 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 4000

Last updated 2020-02-24

No results posted yet for this study

Summary

The goal of the study is to determine whether important clinical outcomes differ among women who access a misoprostol-only medication abortion regimen from a patent medicine vendor when compared with those who access it from a clinic.

Conditions

  • Induced Abortion
  • First Trimester Abortion

Interventions

BEHAVIORAL

Misoprostol sourced from clinics

One cohort of women using misoprostol sourced from clinics

BEHAVIORAL

Misoprostol sourced from PMVs

One cohort of women using misoprostol sourced from PMVs

Sponsors & Collaborators

  • Ipas

    lead OTHER

Eligibility

Min Age
15 Years
Max Age
49 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-05-19
Primary Completion
2020-06-30
Completion
2020-06-30

Countries

  • Nigeria

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 NCT04242212 on ClinicalTrials.gov