At a glance
ClinicalIndex Comparison RecordN/ACompleted· 57 enrolled
Drug / intervention
Copper T380 IUD +1 moredrug
Likely dose
levonorgestrel 1.5 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Pilot Study of Copper T380A IUDs Versus Oral Levonorgestrel for Emergency Contraception
In Brief
A clinical study evaluating Copper T380 IUD and levonorgestrel for Pregnancy. Completed, enrolled 57 participants across 1 site.
Detailed Summary
The purpose of this study is to see if women presenting for emergency contraception (EC) are willing to accept the copper intrauterine device (IUD). This study will also compare the use of effective methods of contraception between women who selected the copper IUD or Plan B 6 months after they received EC.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPregnancy
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartApr 2008
First PostedApr 2008
Primary CompletionApr 2009
Study CompletionMay 2009
TodayJul 2026
First PostedApr 30, 2008
Enrollment StartApr 1, 2008
Primary CompletionApr 1, 2009
Study CompletionMay 1, 2009
TodayJul 2, 2026
Enrollment to primary: 1 yearPosted 18.2 years ago
Interventions
Copper T380 IUDdrug
Copper T380 IUD
levonorgestreldrug
1.5 mg