Oral Contraception Clinical Trial
Official title:
Impact of Pack Supply on Oral Contraception Continuation
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.
Discontinuation of oral contraceptive use in the initial months is common; successful early
continuation is predictive of long term continuation and prevention of unintended pregnancy.
The conventional approach to initiation of hormonal contraceptives in publicly funded
clinics across the United States is to give the patient a limited supply of OCs, or a
prescription with a limited number of refills, and then have her return to the clinic for a
refill. This approach requires the patient to make frequent visits to the clinic, a barrier
to method continuation.
This randomized trial will evaluate a simple but potentially powerful change in family
planning clinic practice, i.e., the effect of dispensing more versus fewer cycles of oral
contraception (OC). The study will be carried out in an urban, publicly funded family
planning clinic that serves a population that is poor, young and primarily Hispanic or
AfricanAmerican. This population was targeted as its members are at increased risk of
discontinuing contraception in the first year of use.
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
Status | Clinical Trial | Phase | |
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Completed |
NCT04901377 -
A Study to Gather Information About User Satisfaction in Women in Russia Who Take Estradiol Valerate/Dienogest
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