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NCT02078414 Clinical Trial

Continued Use of Effective Contraception After Use of Emergency Contraception

Contraception Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02078414
Other study ID # RFSU1
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 2014
Est. completion date May 2015

Study information
Verified date November 2023
Source Karolinska Institutet
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Women using an emergency contraceptive method must use back up protection for 1-2 weeks depending on method. The Copper-IUD is the most effective emergency contraceptive method. The investigators wish to explore if women choosing the Cooper IUD have a higher frequency of use of an effective contraceptive method 3 months and 6 months after the use of an emergency contraceptive method than women who choose to use the emergency contraceptive pill EllaOne (ulipristal acetate).

Recruitment information / eligibility
Status Completed
Enrollment 7
Est. completion date May 2015
Est. primary completion date February 2015
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - women over 18 years - eligible for all emergency contraception Exclusion Criteria: - previous conisation - known stenosis of the cervix - signs of ongoing genital infection - known uterine anomaly - Known bleeding disorder

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Sweden RFSU clinic Stockholm

Sponsors (1)
Lead Sponsor Collaborator
Karolinska Institutet

Country where clinical trial is conducted

Sweden, 

Outcome
Type Measure Description Time frame Safety issue
Primary Use of an effective contraceptive method Use of pill, patch, ring, IUD, IUS, or injection 6 months after use of emergency contraceptive method 6 months after emergency contraceptive use
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