drugset / Trial / NCT00213096
Effects of Hormonal Contraceptives on Liver Proteins and Coagulation Factors: A Comparison of a Contraceptive Vaginal Ring and an Oral Contraceptive
Phase 2
Completed
50 enrolled
Population Council
United States Agency for International Development (USAID) · collab
RandomizedParallel-groupDouble-blindPrevention
Summary
The purpose of this 3-month (cycle) study was to evaluate the effects of hormonal contraceptives containing a progestin and an estrogen on liver proteins and coagulation factors that are sensitive to estrogen. In this study, a contraceptive vaginal ring containing Nestorone® (a progestin with no androgenic properties) and ethinyl estradiol was compared to an oral contraceptive containing levonorgestrel (an androgenic progestin) and ethinyl estradiol.
Timeline
- Start
- 2003-03
- Primary completion
- —
- Completion
- 2004-02
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Levonorgestrel | Small molecule | 150 ug | Oral |
| Subject | Segesterone Acetate | Small molecule | 150 ug | Other |
| Subject | ethinyl estradiol | Small molecule | 15 ug | Other |
| Subject | ethinyl estradiol | Small molecule | 30 ug | Other |
Indications
No indication recorded.