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NCT04599725 Clinical Trial

Feasibility of Telemedicine Medical Abortion

Pregnancy Clinical Trial

Official title:
TelAbortion: Medical Abortion by Direct-to-patient Telemedicine and Mail

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04599725
Other study ID # 1049
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 1, 2020
Est. completion date October 1, 2021

Study information
Verified date October 2020
Source Gynuity Health Projects
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This pilot study is designed to obtain data on the safety, acceptability, and feasibility of providing abortion by direct-to-patient telemedicine and mail.

Recruitment information / eligibility
Status Completed
Enrollment 413
Est. completion date October 1, 2021
Est. primary completion date October 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 10 Years to 50 Years
Eligibility Inclusion Criteria: - desires abortion Exclusion Criteria: - medically ineligible for procedure

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• medical abortion
medical abortion

Locations
Country Name City State
United States Planned Parenthood of the Rocky Mountains Albuquerque New Mexico
United States Carafem Atlanta Georgia
United States Maine Family Planning Augusta Maine
United States Planned Parenthood of Montana Billings Montana
United States Maine Family Planning Boston Massachusetts
United States Carafem Chevy Chase Maryland
United States Planned Parenthood of the Rocky Mountains Denver Colorado
United States The University of Hawaii Women's Options Centers Honolulu Hawaii
United States Emma Goldman Clinic Iowa City Iowa
United States Maine Family Planning New York New York
United States Planned Parenthood Columbia Willamette Portland Oregon
United States Planned Parenthood Minnesota, North Dakota, South Dakota Saint Paul Minnesota
United States Carafem Skokie Illinois
United States Planned Parenthood Columbia Willamette Vancouver Washington
United States Carafem Washington District of Columbia

Sponsors (1)
Lead Sponsor Collaborator
Gynuity Health Projects

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of participants with adverse events 2 years
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