Oral Contraception Clinical Trial
— SixPackOfficial title:
Impact of Pack Supply on Oral Contraception Continuation
Verified date | December 2012 |
Source | Columbia University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The purpose of this study is to determine whether getting more packs of birth control pills leads to improved continuation, when compared with getting the traditional supply.
Status | Completed |
Enrollment | 700 |
Est. completion date | November 2012 |
Est. primary completion date | April 2009 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | N/A to 35 Years |
Eligibility |
Inclusion Criteria: - English or Spanish speaker - age less than or equal to 35 years requesting OC as their primary method of contraception - currently sexually active or anticipating sexual activity within the next 30 days Exclusion Criteria: - contraindications to oral contraceptives per clinic protocol (e.g., hypertension and pregnancy) - currently using OCs (that is, current users requesting a routine refill) - desiring pregnancy within the next 6 months - leaving the clinic catchment area within 6 months - previous participation in this study |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
United States | Columbia University Medical Center, Family Planning Clinic | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Columbia University | Centers for Disease Control and Prevention |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | oral contraception continuation | 6 months | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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