Feasibility of Medical Abortion by Direct-to-Consumer Telemedicine

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

Completed

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Key information

Conditions

Pregnancy

Age range

10 year–50 year

Sex eligibility

Female

Study type

Observational

Primary location

Planned Parenthood of the Rocky Mountains, Denver, Colorado, United States

About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

desires abortion

Exclusion criteria

medically ineligible for procedure

Treatment and study plan

Medical Abortion

Drug

medical abortion

Primary outcomes

Number of participants with adverse events as a measure of safety and tolerability

Time frame: 1 year

adverse events

Sponsors and collaborators

Lead sponsor

Gynuity Health Projects

Other

Registry information

Important dates

Study start: 2016
Primary completion: 2021
Study completion: 2021
First posted: Jul 31, 2015
Registry last updated: Feb 4, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed