Feasibility of Medical Abortion by Direct-to-Consumer Telemedicine

Completed

Conditions studied: Pregnancy

In brief

This pilot study is designed to obtain preliminary data on the safety, acceptability, and feasibility of direct-to-consumer telemedicine abortion.

Key facts

Study ID: NCT02513043
Run by: Gynuity Health Projects
People needed: 1470
Starts: 2016-03-22
Expected to finish: 2021-05-11
Last updated by the study team: 2022-02-04

Who can join

Age: 10 and older, up to 50. Sex: female. Healthy volunteers: accepted.

You may qualify if…

desires abortion

You may not qualify if…

medically ineligible for procedure

Where it is running

Planned Parenthood of the Rocky Mountains — Denver, Colorado, United States
Carafem — Washington D.C., District of Columbia, United States
Carafem — Atlanta, Georgia, United States
The University of Hawaii Women's Options Centers — Honolulu, Hawaii, United States
Carafem — Skokie, Illinois, United States
Emma Goldman Clinic — Iowa City, Iowa, United States
Maine Family Planning — Augusta, Maine, United States
Carafem — Chevy Chase, Maryland, United States
Planned Parenthood Minnesota, North Dakota, South Dakota — Saint Paul, Minnesota, United States
Planned Parenthood of Montana — Billings, Montana, United States
Planned Parenthood of the Rocky Mountains — New Mexico, New Mexico, United States
Choices Women's Medical Center — Jamaica, New York, United States
Maine Family Planning — New York, New York, United States
Planned Parenthood Columbia Willamette — Portland, Oregon, United States
Oregon Health and Sciences University Women's Health Research Unit — Portland, Oregon, United States
Planned Parenthood Columbia Willamette — Washington, Washington, United States
Oregon Health and Sciences University Women's Health Research Unit — Washington, Washington, United States

Full record on ClinicalTrials.gov

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