Feasibility of Medical Abortion by Direct-to-Consumer Telemedicine

NCT02513043 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1470

Last updated 2022-02-04

No results posted yet for this study

Summary

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

Conditions

  • Pregnancy

Interventions

DRUG

medical abortion

medical abortion

Sponsors & Collaborators

  • Gynuity Health Projects

    lead OTHER

Principal Investigators

  • Erica Chong, MPH · Gynuity Health Projects

  • Elizabeth Raymond, MD, MPH · Gynuity Health Projects

Eligibility

Min Age
10 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-03-22
Primary Completion
2021-05-11
Completion
2021-05-11

Countries

  • United States

Study Locations

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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 NCT02513043 on ClinicalTrials.gov