NCT00472394

Brief Summary

New medical abortion regimens are being tested with increasing frequency. However women's preferences for certain attributes of the regimes are not being investigated to any great degree. Consideration of women's preferences in designing new regimens may help to optimize the medical abortion process. The proposed prospective survey research will attempt to determine women's preferences for individual aspects of medical abortion treatment and various regimens, and to determine what attributes of medical abortion treatment may be driving these preferences. The information collected in this study may be used in developing future treatment regimens or as the groundwork for future research into preferences, acceptability, and satisfaction with treatment.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Timeline
Completed

Started Oct 2006

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2006

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

May 10, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

May 11, 2007

Completed
21 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2007

Completed
Last Updated

August 21, 2007

Status Verified

August 1, 2007

First QC Date

May 10, 2007

Last Update Submit

August 17, 2007

Conditions

Medical Abortion

Keywords

Medical abortionPreferencesWillingness to Pay

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Women, aged 18 years or older, who present to the Center for Family Planning Research desiring a medical abortion and are able to read English.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Center for Family Planning Research, Magee-Womens Hospital

Pittsburgh, Pennsylvania, 15213, United States

Location

Study Officials

  • Patricia A Lohr, MD

    University of Pittsuburgh

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Time Perspective
OTHER
Sponsor Type
OTHER

Study Record Dates

First Submitted

May 10, 2007

First Posted

May 11, 2007

Study Start

October 1, 2006

Study Completion

June 1, 2007

Last Updated

August 21, 2007

Record last verified: 2007-08

Locations

US(1)