CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 270 enrolled
Drug / intervention
Copper T-380 IUD +3 moredrug
Likely dose
Not stated in 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.

Search/NCT02076217
NCT02076217N/ACompleted
CompareCT.gov

Rates of Contraceptive Failure When Unprotected Intercourse Has Occurred 6-14 Days Prior to Contraceptive Initiation

University of Utah·observational·Posted Mar 3, 2014·Updated Apr 6, 2026

In Brief

An observational study evaluating Copper T-380 IUD, LNG IUD, and 2 other interventions for IUD and 4 related conditions. Completed, enrolled 270 participants across 1 site.

Detailed Summary

This project will quantify rates of contraceptive failure when unprotected intercourse occurs 6-14 days prior to initiation of highly effective reversible contraceptives (such as IUD's and Implants).

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsIUD, Contraceptive Implant, Contraception, Birth Control, Emergency Contraception
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedMar 3, 2014
Enrollment StartFeb 1, 2014
Primary CompletionOct 1, 2021
TodayJul 2, 2026
Enrollment to primary: 7.7 yearsPosted 12.3 years ago

Interventions

Copper T-380 IUDdrug

LNG IUDdrug

Contraceptive implant Nexplanondevice

Depo-Proveradrug