Exploring the Role of At-home Semi-Quantitative Pregnancy Tests for Medical Abortion Follow-up

NCT01150279 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1200

Last updated 2015-10-02

No results posted yet for this study

Summary

This study will examine the feasibility, acceptability and usability of a semi-quantitative urine pregnancy test (dBest One Step hCG Panel Test Kit) for at-home follow-up after early medical abortion using mifepristone+misoprostol. The study seeks to:

1. Assess the feasibility of using this test in lieu of standard one-week clinic-based follow up for determination of complete abortion status as part of normal service delivery. In Mexico, follow up will be in two weeks, as is standard care in that .
2. To determine if women using this test at home understand how to use it and can correctly interpret the results; is it practical.
3. Assess women's and provider's acceptability of using at-home pregnancy tests in lieu of clinic-based follow up for confirmation of complete medical abortion in the future.

Conditions

  • Medical Abortion

Sponsors & Collaborators

  • Stanford University

    collaborator OTHER
  • Secretaría de Salud del Distrito Federal

    collaborator UNKNOWN
  • Office National de la Famille et de la Population, Tunisia

    collaborator UNKNOWN
  • Maternité de la Rabta, Tunisia

    collaborator UNKNOWN
  • Clinique du Parc, Tunisia

    collaborator UNKNOWN
  • Gynuity Health Projects

    lead OTHER

Principal Investigators

  • Paul D Blumenthal, MD, MPH · Stanford University

  • Beverly Winikoff, MD, MPH · Gynuity Health Projects

  • Jennifer Blum, MPH · Gynuity Health Investigator

  • Patricio Sanhueza Smith, MD · Secretaría de Salud del Distrito Federal

  • Rym Fayala, MD · Office National de la Famille et de la Population

  • Ezzedine Sfar · Maternité de la Rabta

  • Hella Chelli · Clinique du Parc

  • Rasha Dabash, MPH · Gynuity Health Projects

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-08-31
Primary Completion
2014-05-31

Countries

  • United States
  • Mexico
  • Tunisia
  • Vietnam

Study Locations

More Related Trials

Entities

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 NCT01150279 on ClinicalTrials.gov