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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02381223
Other study ID # 1020
Secondary ID
Status Completed
Phase N/A
First received February 23, 2015
Last updated April 28, 2017
Start date March 2015
Est. completion date January 2017

Study information

Verified date April 2017
Source Gynuity Health Projects
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to collection additional data on the safety and acceptability of medical abortion without pretreatment pelvic ultrasound or exam in woman who meet certain criteria.


Recruitment information / eligibility

Status Completed
Enrollment 409
Est. completion date January 2017
Est. primary completion date January 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion criteria:

- Women having medical abortion

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Mexico Centro de Salud Mexico-Espana Mexico Distrito Federal
Moldova, Republic of Reproductive Health Training Center Chisinau
United States Carafem Friendship Heights Maryland
United States Planned Parenthood Minnesota, North Dakota, South Dakora Minneapolis Minnesota
United States Institute for Family Health New York New York

Sponsors (1)

Lead Sponsor Collaborator
Gynuity Health Projects

Countries where clinical trial is conducted

United States,  Mexico,  Moldova, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of serious adverse events 7 days
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Not yet recruiting NCT04194658 - Effectiveness of Pretreatment Letrozole Versus Misoprostol Alone in Missed Abortion Phase 2
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Completed NCT01966874 - Mifepristone and Misoprostol for the Termination of Pregnancy up to 70 Days Gestation Phase 2/Phase 3