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Clinical Trial Summary

As intrauterine contraception is an increasingly popular form of contraception the objective of our study is to examine if uterine size or posture affects the insertion or use of intrauterine devices. Nulliparous women requesting either the levonorgestrel-releasing device (LNG-IUS) or a copper-IUD (NovaT) are recruited and followed for one year.


Clinical Trial Description

Prospective observational study among nulliparous women requesting intrauterine contraception. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01685164
Study type Observational
Source Helsinki University Central Hospital
Contact
Status Completed
Phase N/A
Start date January 2011
Completion date July 2013

See also
  Status Clinical Trial Phase
Completed NCT01022645 - Postpartum Glucose Tolerance With Levonorgesterel IUD Use in Women With Recent Gestational Diabetes Phase 4
Not yet recruiting NCT05343546 - Ideal Timing of Intrauterine Contraception Insertion After Medical Management of First Trimester Incomplete Abortion N/A