Misoprostol Prior to Intrauterine Device (IUD) Insertion in Nulliparous Women
Completed · Not applicable · Has a placebo group
Conditions studied: Contraception
In brief
The purpose of this study is to see if inserting misoprostol in the vagina or between your cheek and gum before inserting an Intrauterine Device (IUD) in a woman who has never had a baby makes it easier and less painful.
Key facts
- Study ID
- NCT00886834
- Run by
- University of Utah
- People needed
- 108
- Starts
- 2009-04-01
- Expected to finish
- 2011-03-01
- Last updated by the study team
- 2014-12-22
Who can join
Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- 18 years old or older
- negative pregnancy test
- no prior pregnancies beyond 14 6/7 weeks
- no PID in last 3 months
- no current cervicitis
- be willing to follow-up in 1-2 months for an IUD string check.
You may not qualify if…
- active cervical infection
- current pregnancy
- prior pregnancy beyond 14 weeks gestation
- known uterine anomaly
- fibroid uterus distorting uterine cavity
- copper allergy/Wilson's disease (for Paragard)
- undiagnosed abnormal uterine bleeding
- cervical or uterine cancer.
Where it is running
- Planned Parenthood Association of Utah — Salt Lake City, Utah, United States
- University of Utah — Salt Lake City, Utah, United States
Full record on ClinicalTrials.gov
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