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Feasibility of Medical Abortion by Direct-to-Consumer Telemedicine

Feasibility of Medical Abortion by Direct-to-Consumer Telemedicine

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02513043
Enrollment
1470
Registered
2015-07-31
Start date
2016-03-22
Completion date
2021-05-11
Last updated
2022-02-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy

Brief summary

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

Detailed description

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

Interventions

DRUGmedical abortion

medical abortion

Sponsors

Gynuity Health Projects
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
10 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* desires abortion

Exclusion criteria

* medically ineligible for procedure

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with adverse events as a measure of safety and tolerability1 yearadverse events

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026