Clinical Trials Directory

Trials / Completed

CompletedNCT00120913

Continuous Oral Contraceptives (COCs): Are Bleeding Patterns Dependent on the Hormones Given?

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
160 (planned)
Sponsor
Oregon Health and Science University · Academic / Other
Sex
Female
Age
18 Years – 49 Years
Healthy volunteers
Accepted

Summary

While there may be a decrease in the total number of bleeding days women experience with continuous-dosed COCs (no menstrual withdrawal week), these regimens frequently result in an increased number of "breakthrough" or non-scheduled bleeding days. Breakthrough bleeding is among the main reasons cited for discontinuation of combined COCs dosed traditionally (3 weeks of active pill, 1 week of placebo) or continuously, and may offset the perceived benefit of fewer withdrawal bleeding events for many women taking continuous-dosed COCs. The exact mechanisms responsible for breakthrough bleeding patterns during hormonal contraception are unknown and may be related to the pill formulation. This study is to determine whether progestin type or estrogen dose influences bleeding patterns, side effects, or satisfaction with combined oral contraceptives (COC) dosed continuously.

Conditions

Interventions

TypeNameDescription
DRUGBirth control pills

Timeline

Completion
2004-08-01
First posted
2005-07-19
Last updated
2005-07-19

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00120913. Inclusion in this directory is not an endorsement.

Continuous Oral Contraceptives (COCs): Are Bleeding Patterns Dependent on the Hormones Given? (NCT00120913) · Clinical Trials Directory