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OpenTrials
Completed

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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Key information

Conditions

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

Centro de Salud Beatriz Velasco de Aleman, Mexico City, Mexico

Loading trial locations.

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

Timing of Contraceptive Initiation in Medical Abortion

Other

Primary outcomes

  1. Medical Abortion Failure

    Time frame: One month after enrollment

  2. 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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