NCT Number: NCT01902485
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
This study will compare immediate to post-abortion start of two progestin-based contraceptives (DMPA and etonorgestrel implants) among women having first trimester medical abortion who wish to use that method for post-abortion contraception.
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Notify MeKey information
Conditions
Sex eligibility
Female
Study type
Interventional
Phase
Phase 4
Primary location
Centro de Salud Beatriz Velasco de Aleman, Mexico City, Mexico
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Women having medical abortion desiring progestin-based contraceptives (injectables or implants)
Treatment and study plan
Primary outcomes
-
Medical Abortion Failure
Time frame: One month after enrollment
-
Repeat Pregnancy
Time frame: 6 months after enrollment
Sponsors and collaborators
Lead sponsor
Gynuity Health Projects
Other
Registry information
Official study title
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Acronym: Quickstart
Important dates
- Study start
- 2013
- Primary completion
- 2015
- Study completion
- 2015
- First posted
- Jul 18, 2013
- Registry last updated
- Mar 4, 2016
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.
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