Contraception Clinical Trial
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 |
Verified date | November 2023 |
Source | Karolinska Institutet |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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).
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 |
Country | Name | City | State |
---|---|---|---|
Sweden | RFSU clinic | Stockholm |
Lead Sponsor | Collaborator |
---|---|
Karolinska Institutet |
Sweden,
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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