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Study of the Copper IUD or Oral Levonorgestrel and the Levonorgestrel IUD for Women Seeking Emergency Contraception

NCT01963962 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 188

Last updated 2016-08-08

No results posted yet for this study

Summary

The purpose of this study is to see how often women who come to a family planning clinic for emergency contraception, the morning after pill, are willing to use either the copper IUD or the levonorgestrel IUD. The investigators will also see if pregnancies occur in those choosing the levonorgestrel IUD and if people continue to use the IUD for 1 year.

Conditions

  • Emergency Contraception

Interventions

DRUG

Copper IUD

DRUG

Levonorgestrel IUD

Sponsors & Collaborators

Principal Investigators

  • David Turok, MD · University of Utah

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-07-31
Primary Completion
2016-02-29
Completion
2016-02-29

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01963962 on ClinicalTrials.gov